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97 jobs found in pleasant prairie, wisconsin

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    • lake bluff, illinois
    • temp to perm
    • $16 - $17.50 per hour
    A home improvment supplies distribution company in Lake Bluff, IL & North Chicago, IL. is looking for entry level position candidates to help building displays and unloading containers/ some Pick and Pack. Candidates must be physically able to lift 50lbs consistantly. This is a 2nd shift position working Monday-Friday for $17.50/hr. If you or anyone you know is interested in this opportunity, please apply today and be scheduled for a phone interview with one of our recruiters immediatley.  -Immediate start -Weekly Pay DON'T MISS OUT! salary: $16 - $17.5 per hourshift: Secondwork hours: 2:30 PM - 11 PMeducation: High` SchoolResponsibilities Able to lift up to 50lbs continuously  Fast pace work Stacking boxes on pallets Wrapping Pallets  Building displays & filling with product  Order picking using a pick sheet RF Scanner Push/Pull Pallet Jack The essential functions of this role include:working in a smoke free environmentmanual lifting up to 50lbsstanding for 8 hours at one timeSkillsPackingPalletizingLiftingStackingOrder PickingOrder PullingQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    A home improvment supplies distribution company in Lake Bluff, IL & North Chicago, IL. is looking for entry level position candidates to help building displays and unloading containers/ some Pick and Pack. Candidates must be physically able to lift 50lbs consistantly. This is a 2nd shift position working Monday-Friday for $17.50/hr. If you or anyone you know is interested in this opportunity, please apply today and be scheduled for a phone interview with one of our recruiters immediatley.  -Immediate start -Weekly Pay DON'T MISS OUT! salary: $16 - $17.5 per hourshift: Secondwork hours: 2:30 PM - 11 PMeducation: High` SchoolResponsibilities Able to lift up to 50lbs continuously  Fast pace work Stacking boxes on pallets Wrapping Pallets  Building displays & filling with product  Order picking using a pick sheet RF Scanner Push/Pull Pallet Jack The essential functions of this role include:working in a smoke free environmentmanual lifting up to 50lbsstanding for 8 hours at one timeSkillsPackingPalletizingLiftingStackingOrder PickingOrder PullingQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • contract
    • $30 - $35.40 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $30.00 - 35.40 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Regulatory Affairs Analyst, reviews, and assess incoming global regulatory information for entry into Company's registration and documentation management systems.Interacts with all areas of regulatory affairs and affiliates to ensure registration management information is current, accurate and available in regulatory systems.Executes established business processes and may assist in development and implementation of process/system changes and/or data remediation projects. Troubleshoots errors and system performance issues and works with supervisor and IT on business problem resolution and enhancements.Participates and contributes to group, department, and cross-functional meetings.May also assist in training junior team members.  qualifications: Bachelor's Degree, 4+ years in a related area including manufacturing, regulatory affairs, R&D, or quality in the pharmaceutical, medical device, or other healthcare industry.Experience/understanding/use of software tools.Demonstrated analytical and communication skills.Skills and knowledge of drug submissions  skills: IND, FDA, MS-WORD, MS-EXCEL, Submissions, ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $30.00 - 35.40 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Regulatory Affairs Analyst, reviews, and assess incoming global regulatory information for entry into Company's registration and documentation management systems.Interacts with all areas of regulatory affairs and affiliates to ensure registration management information is current, accurate and available in regulatory systems.Executes established business processes and may assist in development and implementation of process/system changes and/or data remediation projects. Troubleshoots errors and system performance issues and works with supervisor and IT on business problem resolution and enhancements.Participates and contributes to group, department, and cross-functional meetings.May also assist in training junior team members.  qualifications: Bachelor's Degree, 4+ years in a related area including manufacturing, regulatory affairs, R&D, or quality in the pharmaceutical, medical device, or other healthcare industry.Experience/understanding/use of software tools.Demonstrated analytical and communication skills.Skills and knowledge of drug submissions  skills: IND, FDA, MS-WORD, MS-EXCEL, Submissions, ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois (remote)
    • contract
    • $35 - $41 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $35 - 41 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and Company policies and procedures).Supports the Study Project Manager in leading the cross functional study team: Supports the preparation of Clinical Study Team meetings (Agenda/Minutes)Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date Supports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR)Supports the vendor selection, scope development, management and oversight of external vendors in compliance with Company's processes and procedures and the applicable regulations.Responsible for generating the study related training for the study team, study sites, and vendors for assigned studiesProactively identify and resolve and/or escalate study related issuesParticipates in process improvement initiatives  qualifications: Bachelor's Degree or OUS equivalent degree required, typically in nursing or scientific field; Registered Nurse licensure with Associate's Degree in Nursing with relevant experience is also acceptable.Must have at least four years of Pharma-related/clinical research related experience and demonstrated a high level of core and technical competencies.Experience working in oncology and/or working with CRO preferred.Possesses good communication skills.Competent in application of standard business procedures {Standard operating procedures, International Conference on Harmonization {ICH), Global Regulations, Ethics and Compliance).Preferred exposure to study initiation through study completion.  skills: Phase I, Phase II, Phase iii, Phase iv, MS-WORD, MS-EXCEL, MS-Powerpoint, CRFs, GCP (Good Clinical Practice), CTMS (Clinical Trial Management Systems), ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $35 - 41 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and Company policies and procedures).Supports the Study Project Manager in leading the cross functional study team: Supports the preparation of Clinical Study Team meetings (Agenda/Minutes)Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date Supports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR)Supports the vendor selection, scope development, management and oversight of external vendors in compliance with Company's processes and procedures and the applicable regulations.Responsible for generating the study related training for the study team, study sites, and vendors for assigned studiesProactively identify and resolve and/or escalate study related issuesParticipates in process improvement initiatives  qualifications: Bachelor's Degree or OUS equivalent degree required, typically in nursing or scientific field; Registered Nurse licensure with Associate's Degree in Nursing with relevant experience is also acceptable.Must have at least four years of Pharma-related/clinical research related experience and demonstrated a high level of core and technical competencies.Experience working in oncology and/or working with CRO preferred.Possesses good communication skills.Competent in application of standard business procedures {Standard operating procedures, International Conference on Harmonization {ICH), Global Regulations, Ethics and Compliance).Preferred exposure to study initiation through study completion.  skills: Phase I, Phase II, Phase iii, Phase iv, MS-WORD, MS-EXCEL, MS-Powerpoint, CRFs, GCP (Good Clinical Practice), CTMS (Clinical Trial Management Systems), ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • pleasant prairie, wisconsin
    • temp to perm
    • $18 - $18.50 per hour
    Are you an experienced forklift operator looking for a long term role with opportunity to grow?  Randstad is looking to fill multiple roles in a busy distribution center in Pleasant Prairie, WI! Job will entail loading trucks, unloading trucks and movement of goods around the facility.  These temp to perm roles pay $18-$18.50/hr pending the shift!  12 hr shifts, 4 days a week!  Must meet the following requirements:  -Ability to pass background/drug screen -At least 6 months of forklift operation in the last 3 years -Ability to pass online forklift exam  salary: $18 - $18.5 per hourshift: Firstwork hours: 4 AM - 4 PMeducation: No Degree RequiredResponsibilitiesPositions entail: Unloading trucks Picking orders Replenishing product in warehouse Loading trucks You will use a WMS system and operate the forklift to safely and efficiently move product in the warehouse. The essential functions of this role include:working in a smoke free environmentwearing steel toe shoesmanual lifting up to 50lbsstanding for 12 hours at one timeworking up to 10 hrs of overtime per weekworking weekendsSkillsCherry PickingStand Up ForkliftsSit Down ForkliftsMaterial HandlingReach Truck OperationTime ManagementOrder ProcessingMoving MaterialQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Are you an experienced forklift operator looking for a long term role with opportunity to grow?  Randstad is looking to fill multiple roles in a busy distribution center in Pleasant Prairie, WI! Job will entail loading trucks, unloading trucks and movement of goods around the facility.  These temp to perm roles pay $18-$18.50/hr pending the shift!  12 hr shifts, 4 days a week!  Must meet the following requirements:  -Ability to pass background/drug screen -At least 6 months of forklift operation in the last 3 years -Ability to pass online forklift exam  salary: $18 - $18.5 per hourshift: Firstwork hours: 4 AM - 4 PMeducation: No Degree RequiredResponsibilitiesPositions entail: Unloading trucks Picking orders Replenishing product in warehouse Loading trucks You will use a WMS system and operate the forklift to safely and efficiently move product in the warehouse. The essential functions of this role include:working in a smoke free environmentwearing steel toe shoesmanual lifting up to 50lbsstanding for 12 hours at one timeworking up to 10 hrs of overtime per weekworking weekendsSkillsCherry PickingStand Up ForkliftsSit Down ForkliftsMaterial HandlingReach Truck OperationTime ManagementOrder ProcessingMoving MaterialQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lake forest, illinois
    • permanent
    • $110,000 - $125,000 per year
    job summary: The Senior Embedded Software Engineer will work closely with software engineering peers and leads to identify requirements-related issues and explore alternative resolutions. They will work with cross-functional team members consisting of Technical Spec Writers, Marketing, Medical, Regulatory, Program, Software Development and Software Test Management. This position is responsible for assisting with the design and development of test software for Board Support Package for next generation products   location: Lake Forest, Illinois job type: Permanent salary: $110,000 - 125,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Participate in Board Support Package (BSP) software design & overall system architecture covering features, functionality, reliability, and performance.Function as a senior level individual contributor that works well with minimum direction on assigned tasks. Seeks guidance/clarification as required.Participate in Product and BSP software requirements definition and requirements process development. Assess Cross-disciplinary requirements and design trade-offs.Participate in Risk identification, assessment and mitigation, including assisting the creation of hazards analysis investigation and failure mode analysis.Identify approaches; make recommendations for BSP software design & development.Participate in Root cause analysis of field related issuesDevelop Test tools for supporting CE 3.0 in factory.Support WiFi regulatory tests.Monitor WiFi standards to ensure compliance on products.   qualifications: Experience level: ExperiencedMinimum 7 years of experienceEducation: Bachelors (required)  skills: Embedded Coding (4 years of experience is required)Board Support Package (4 years of experience is required)Linux Kernel (4 years of experience is required)Python (4 years of experience is preferred)C++ (4 years of experience is preferred) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Senior Embedded Software Engineer will work closely with software engineering peers and leads to identify requirements-related issues and explore alternative resolutions. They will work with cross-functional team members consisting of Technical Spec Writers, Marketing, Medical, Regulatory, Program, Software Development and Software Test Management. This position is responsible for assisting with the design and development of test software for Board Support Package for next generation products   location: Lake Forest, Illinois job type: Permanent salary: $110,000 - 125,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Participate in Board Support Package (BSP) software design & overall system architecture covering features, functionality, reliability, and performance.Function as a senior level individual contributor that works well with minimum direction on assigned tasks. Seeks guidance/clarification as required.Participate in Product and BSP software requirements definition and requirements process development. Assess Cross-disciplinary requirements and design trade-offs.Participate in Risk identification, assessment and mitigation, including assisting the creation of hazards analysis investigation and failure mode analysis.Identify approaches; make recommendations for BSP software design & development.Participate in Root cause analysis of field related issuesDevelop Test tools for supporting CE 3.0 in factory.Support WiFi regulatory tests.Monitor WiFi standards to ensure compliance on products.   qualifications: Experience level: ExperiencedMinimum 7 years of experienceEducation: Bachelors (required)  skills: Embedded Coding (4 years of experience is required)Board Support Package (4 years of experience is required)Linux Kernel (4 years of experience is required)Python (4 years of experience is preferred)C++ (4 years of experience is preferred) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • contract
    • $16 - $17 per hour
    job summary: Randstad Technologies is hiring and we're looking for someone like YOU to join our team! If you are seeking a new opportunity, looking to grow in your career, or you know someone who is - we want to hear from you! Take a look at the below opportunity, or feel free to visit RandstadUSA.com to view and apply to any of our open roles.   location: Waukegan, Illinois job type: Contract salary: $16 - 17 per hour work hours: 8am to 4pm education: No Degree Required   responsibilities: Respond to all incoming contacts (phone/email/online). Document incident/request specifics in the Incident Management System. Triage/troubleshoot/diagnose/resolve incidents through use of experience, available documentation and tools. Expected resolution rate is outlined in section 6.4 Service Level Objectives. Document all relevant data on issue unable to resolve (including incident specifics and any actions taken to attempt to resolve) and escalate to appropriate Service Desk or ITG support team. Triage outage assessed as being critical/high priority and follow procedures to escalate the incident to the Tactical Response Unit team. Communicate any current outage/critical incident status to callers and, if new information/symptoms reported, communicate to the tactical response unit to update team on technical bridge. Participate in continuous process improvement activities, making recommendations whenever possible. Participate in project work Comply with HIPAA, diversity principles, corporate integrity, compliance program policies and other applicable corporate and departmental policies. Maintain complete confidentiality of company related business. Maintain effective communication with management regarding development within areas of assigned responsibilities and perform special projects as required or requested. Technical certification/diploma with 1 years experience in a technical call center, customer service team or service desk OR 3 years experience in a technical call center, customer service team or service desk. Verbal, written, interpersonal, team-building, organizational and customer service skills. Troubleshooting and problem solving skills. Support 24/7 hours of operation. Proficiency in typing   qualifications: Experience level: Entry LevelMinimum 1 year of experienceEducation: No Degree Required  skills: Help Desk SupportMS OfficeTicketingWindows (1 year of experience is required)VPN (1 year of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Randstad Technologies is hiring and we're looking for someone like YOU to join our team! If you are seeking a new opportunity, looking to grow in your career, or you know someone who is - we want to hear from you! Take a look at the below opportunity, or feel free to visit RandstadUSA.com to view and apply to any of our open roles.   location: Waukegan, Illinois job type: Contract salary: $16 - 17 per hour work hours: 8am to 4pm education: No Degree Required   responsibilities: Respond to all incoming contacts (phone/email/online). Document incident/request specifics in the Incident Management System. Triage/troubleshoot/diagnose/resolve incidents through use of experience, available documentation and tools. Expected resolution rate is outlined in section 6.4 Service Level Objectives. Document all relevant data on issue unable to resolve (including incident specifics and any actions taken to attempt to resolve) and escalate to appropriate Service Desk or ITG support team. Triage outage assessed as being critical/high priority and follow procedures to escalate the incident to the Tactical Response Unit team. Communicate any current outage/critical incident status to callers and, if new information/symptoms reported, communicate to the tactical response unit to update team on technical bridge. Participate in continuous process improvement activities, making recommendations whenever possible. Participate in project work Comply with HIPAA, diversity principles, corporate integrity, compliance program policies and other applicable corporate and departmental policies. Maintain complete confidentiality of company related business. Maintain effective communication with management regarding development within areas of assigned responsibilities and perform special projects as required or requested. Technical certification/diploma with 1 years experience in a technical call center, customer service team or service desk OR 3 years experience in a technical call center, customer service team or service desk. Verbal, written, interpersonal, team-building, organizational and customer service skills. Troubleshooting and problem solving skills. Support 24/7 hours of operation. Proficiency in typing   qualifications: Experience level: Entry LevelMinimum 1 year of experienceEducation: No Degree Required  skills: Help Desk SupportMS OfficeTicketingWindows (1 year of experience is required)VPN (1 year of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • contract
    • $16 - $17 per hour
    job summary: Randstad Technologies is hiring and we're looking for someone like YOU to join our team! If you are seeking a new opportunity, looking to grow in your career, or you know someone who is - we want to hear from you! Take a look at the below opportunity, or feel free to visit RandstadUSA.com to view and apply to any of our open roles.   location: Waukegan, Illinois job type: Contract salary: $16 - 17 per hour work hours: 8am to 4pm education: No Degree Required   responsibilities: Respond to all incoming contacts (phone/email/online). Document incident/request specifics in the Incident Management System. Triage/troubleshoot/diagnose/resolve incidents through use of experience, available documentation and tools. Expected resolution rate is outlined in section 6.4 Service Level Objectives. Document all relevant data on issue unable to resolve (including incident specifics and any actions taken to attempt to resolve) and escalate to appropriate Service Desk or ITG support team. Triage outage assessed as being critical/high priority and follow procedures to escalate the incident to the Tactical Response Unit team. Communicate any current outage/critical incident status to callers and, if new information/symptoms reported, communicate to the tactical response unit to update team on technical bridge. Participate in continuous process improvement activities, making recommendations whenever possible. Participate in project work Comply with HIPAA, diversity principles, corporate integrity, compliance program policies and other applicable corporate and departmental policies. Maintain complete confidentiality of company related business. Maintain effective communication with management regarding development within areas of assigned responsibilities and perform special projects as required or requested. Technical certification/diploma with 1 years experience in a technical call center, customer service team or service desk OR 3 years experience in a technical call center, customer service team or service desk. Verbal, written, interpersonal, team-building, organizational and customer service skills. Troubleshooting and problem solving skills. Support 24/7 hours of operation. Proficiency in typing   qualifications: Experience level: Entry LevelMinimum 1 year of experienceEducation: No Degree Required  skills: Help Desk SupportMS OfficeTicketingWindows (1 year of experience is required)VPN (1 year of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Randstad Technologies is hiring and we're looking for someone like YOU to join our team! If you are seeking a new opportunity, looking to grow in your career, or you know someone who is - we want to hear from you! Take a look at the below opportunity, or feel free to visit RandstadUSA.com to view and apply to any of our open roles.   location: Waukegan, Illinois job type: Contract salary: $16 - 17 per hour work hours: 8am to 4pm education: No Degree Required   responsibilities: Respond to all incoming contacts (phone/email/online). Document incident/request specifics in the Incident Management System. Triage/troubleshoot/diagnose/resolve incidents through use of experience, available documentation and tools. Expected resolution rate is outlined in section 6.4 Service Level Objectives. Document all relevant data on issue unable to resolve (including incident specifics and any actions taken to attempt to resolve) and escalate to appropriate Service Desk or ITG support team. Triage outage assessed as being critical/high priority and follow procedures to escalate the incident to the Tactical Response Unit team. Communicate any current outage/critical incident status to callers and, if new information/symptoms reported, communicate to the tactical response unit to update team on technical bridge. Participate in continuous process improvement activities, making recommendations whenever possible. Participate in project work Comply with HIPAA, diversity principles, corporate integrity, compliance program policies and other applicable corporate and departmental policies. Maintain complete confidentiality of company related business. Maintain effective communication with management regarding development within areas of assigned responsibilities and perform special projects as required or requested. Technical certification/diploma with 1 years experience in a technical call center, customer service team or service desk OR 3 years experience in a technical call center, customer service team or service desk. Verbal, written, interpersonal, team-building, organizational and customer service skills. Troubleshooting and problem solving skills. Support 24/7 hours of operation. Proficiency in typing   qualifications: Experience level: Entry LevelMinimum 1 year of experienceEducation: No Degree Required  skills: Help Desk SupportMS OfficeTicketingWindows (1 year of experience is required)VPN (1 year of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • permanent
    • $70,000 - $80,000 per year
    job summary: HPI Production Support Supervisor Waukegan, IL 24/7 Operation - 1 st shift, but open to work 2 nd shift when required. 12 hour shift - Rotating - 5:30am-5:30pm or 5:30pm-5:30am Example - Work Sun, Off Mon/Tues, Work Wed/Thurs, Off Fri, Sat Looking for at least 5-7 years of exp JOB SUMMARY The Shift Production Supervisor will be responsible for leading a team of manufacturing operators in a team environment and assisting with the manufacture of pharmaceutical products while following cGMP protocol and ensuring a safe, quality, compliant and cost efficient operation. A collaborative working relationship with other Shift Supervisors, the Production Manager and other key groups to help us maintain a cGMP facility dedicated to providing the highest quality product to our customers.   location: Waukegan, Illinois job type: Permanent salary: $70,000 - 80,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES Learn and become proficient in all aspects of all unit operations in the production of HPI products.Leading the Operation's Department cGMP deviation investigations, Corrective Action Preventive Actions (CAPA), Investigations, Resolution, and Documentation.Responsible for departmental document periodic review and document control request (DCR) initiation and finalizationResponsible for conducting and overseeing Batch Record (PBR) and Standard Operating Procedure Reviews. Including developing and administrating an operational continuous improvement methodology for 'fixes' that are slowing down the PBR, Pre-Quality Assurance Review process.Training HPI operators on key pieces equipment - i.e. Ultra Filter, RO Water, etc.Training to include instilling the company culture of Quality, Safety and Delivery. When acting in a Support Supervisor capacity: Supervise personnel/resources for manufacturing of Bulk Pharmaceutical High Purity Ingredients (HPI) regulated by the Food and Drug Administration (FDA) according to current Good Manufacturing Practices (cGMP) regulations and ICH guidelines in accordance with Quality policy and Standard Operating Procedures (SOPs) to accomplish all departmental goals and objectives while operating in a safe manner and in compliance with all applicable regulations. Understanding all manufacturing systems within the production space, including knowledge of ancillary equipment such as storage and distribution systems, waste neutralization systems, heating/cooling units, vacuum units, etc.Ensure tasks are completed in accordance with approved site procedures, batch records, and protocols.Completes, reviews, and corrects critical documentation including SOP Forms, Batch Records, Logbooks, etc., to ensure completeness and accuracy in compliance with all applicable procedures and ensuring quality documentation under good manufacturing and documentation practices.Ensure all Cleaning and Process validation work is done within allotted timeline.Interface with Supply Chain to ensure adherence to production schedule and the development of said schedule.Coordinate manufacturing needs with other departments and ensure efficient operation of the reactor systems and ancillary production support equipment.Ensure that the production area is maintained, organized and cleaned on a daily basis per SOP's including packaging area.Troubleshooting equipment problems and assisting operators in basic troubleshooting.Overseeing small maintenance repairs and using organization's work order system for maintenance or improvement requests.Aid in selection, training, developing, motivating, and evaluating employees.Develop employee's knowledge, understanding, and skills to improve performance and expand abilities.Ensure employees remain current with all department and site training requirements.Complete performance reviews for direct reports and review job descriptions on an annual basis.Taking an active role in incident inquiry, investigation, and reporting.Communicate the group's status, data and feedback to management.Other tasks as needed by the company.  qualifications: EDUCATION / EXPERIENCE Education : High School Diploma or equivalent required. Bachelor of Science in Chemistry or Chemical Engineering preferred. Experience : Minimum 5-7 years of manufacturing experience in fine chemicals and pharmaceutical compounds. Prior experience supervising in a fine chemicals and/or pharmaceutical compounds manufacturing environment preferred. Current knowledge of current OSHA, Employment Law, and cGMP regulations required.Working experience with Continuous Improvement and/or Lean Six Sigma methodologies.Exceptional interpersonal skills.Prior experience supervising in a union environment helpful.Working knowledge of Microsoft Office Suite required. PHYSICAL REQUIREMENTS Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plant.Must be able to sit and/or stand for extended periods.Ability to work effectively under pressure to meet deadlines.Frequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, and listening.Must be able to lift 50 lbs.Ability to wear proper safety equipment when working in the plant.  skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: HPI Production Support Supervisor Waukegan, IL 24/7 Operation - 1 st shift, but open to work 2 nd shift when required. 12 hour shift - Rotating - 5:30am-5:30pm or 5:30pm-5:30am Example - Work Sun, Off Mon/Tues, Work Wed/Thurs, Off Fri, Sat Looking for at least 5-7 years of exp JOB SUMMARY The Shift Production Supervisor will be responsible for leading a team of manufacturing operators in a team environment and assisting with the manufacture of pharmaceutical products while following cGMP protocol and ensuring a safe, quality, compliant and cost efficient operation. A collaborative working relationship with other Shift Supervisors, the Production Manager and other key groups to help us maintain a cGMP facility dedicated to providing the highest quality product to our customers.   location: Waukegan, Illinois job type: Permanent salary: $70,000 - 80,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES Learn and become proficient in all aspects of all unit operations in the production of HPI products.Leading the Operation's Department cGMP deviation investigations, Corrective Action Preventive Actions (CAPA), Investigations, Resolution, and Documentation.Responsible for departmental document periodic review and document control request (DCR) initiation and finalizationResponsible for conducting and overseeing Batch Record (PBR) and Standard Operating Procedure Reviews. Including developing and administrating an operational continuous improvement methodology for 'fixes' that are slowing down the PBR, Pre-Quality Assurance Review process.Training HPI operators on key pieces equipment - i.e. Ultra Filter, RO Water, etc.Training to include instilling the company culture of Quality, Safety and Delivery. When acting in a Support Supervisor capacity: Supervise personnel/resources for manufacturing of Bulk Pharmaceutical High Purity Ingredients (HPI) regulated by the Food and Drug Administration (FDA) according to current Good Manufacturing Practices (cGMP) regulations and ICH guidelines in accordance with Quality policy and Standard Operating Procedures (SOPs) to accomplish all departmental goals and objectives while operating in a safe manner and in compliance with all applicable regulations. Understanding all manufacturing systems within the production space, including knowledge of ancillary equipment such as storage and distribution systems, waste neutralization systems, heating/cooling units, vacuum units, etc.Ensure tasks are completed in accordance with approved site procedures, batch records, and protocols.Completes, reviews, and corrects critical documentation including SOP Forms, Batch Records, Logbooks, etc., to ensure completeness and accuracy in compliance with all applicable procedures and ensuring quality documentation under good manufacturing and documentation practices.Ensure all Cleaning and Process validation work is done within allotted timeline.Interface with Supply Chain to ensure adherence to production schedule and the development of said schedule.Coordinate manufacturing needs with other departments and ensure efficient operation of the reactor systems and ancillary production support equipment.Ensure that the production area is maintained, organized and cleaned on a daily basis per SOP's including packaging area.Troubleshooting equipment problems and assisting operators in basic troubleshooting.Overseeing small maintenance repairs and using organization's work order system for maintenance or improvement requests.Aid in selection, training, developing, motivating, and evaluating employees.Develop employee's knowledge, understanding, and skills to improve performance and expand abilities.Ensure employees remain current with all department and site training requirements.Complete performance reviews for direct reports and review job descriptions on an annual basis.Taking an active role in incident inquiry, investigation, and reporting.Communicate the group's status, data and feedback to management.Other tasks as needed by the company.  qualifications: EDUCATION / EXPERIENCE Education : High School Diploma or equivalent required. Bachelor of Science in Chemistry or Chemical Engineering preferred. Experience : Minimum 5-7 years of manufacturing experience in fine chemicals and pharmaceutical compounds. Prior experience supervising in a fine chemicals and/or pharmaceutical compounds manufacturing environment preferred. Current knowledge of current OSHA, Employment Law, and cGMP regulations required.Working experience with Continuous Improvement and/or Lean Six Sigma methodologies.Exceptional interpersonal skills.Prior experience supervising in a union environment helpful.Working knowledge of Microsoft Office Suite required. PHYSICAL REQUIREMENTS Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plant.Must be able to sit and/or stand for extended periods.Ability to work effectively under pressure to meet deadlines.Frequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, and listening.Must be able to lift 50 lbs.Ability to wear proper safety equipment when working in the plant.  skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • permanent
    • $90,000 - $100,000 per year
    job summary: HPI Production Supervisor Waukegan, IL 24/7 Operation - 1 st shift, but open to work 2 nd shift when required. 12 hour shift - Rotating - 5:30am-5:30pm or 5:30pm-5:30am Example - Work Sun, Off Mon/Tues, Work Wed/Thurs, Off Fri, Sat   location: Waukegan, Illinois job type: Permanent salary: $90,000 - 100,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: JOB SUMMARY The Shift Production Supervisor will be responsible for leading a team of manufacturing operators in a team environment and assisting with the manufacture of pharmaceutical products while following cGMP protocol and ensuring a safe, quality, compliant and cost efficient operation. A collaborative working relationship with other Shift Supervisors, the Production Manager and other key groups to help us maintain a cGMP facility dedicated to providing the highest quality product to our customers. ESSENTIAL DUTIES AND RESPONSIBILITIES Supervise personnel/resources for manufacturing of Bulk Pharmaceutical High Purity Ingredients (HPI) regulated by the Food and Drug Administration (FDA) according to current Good Manufacturing Practices (cGMP) regulations and ICH guidelines in accordance with Quality policy and Standard Operating Procedures (SOPs) to accomplish all departmental goals and objectives while operating in a safe manner and in compliance with all applicable regulations.Understanding all manufacturing systems within the production space, including knowledge of ancillary equipment such as storage and distribution systems, waste neutralization systems, heating/cooling units, vacuum units, etc.Ensure tasks are completed in accordance with approved site procedures, batch records, and protocols.Completes, reviews, and corrects critical documentation including SOP Forms, Batch Records, Logbooks, etc., to ensure completeness and accuracy in compliance with all applicable procedures and ensuring quality documentation under good manufacturing and documentation practices.Ensure all Cleaning and Process validation work is done within allotted timeline.Interface with Supply Chain to ensure adherence to production schedule and the development of said schedule.Coordinate manufacturing needs with other departments and ensure efficient operation of the reactor systems and ancillary production support equipment.Ensure that the production area is maintained, organized and cleaned on a daily basis per SOP's including packaging area.Troubleshooting equipment problems and assisting operators in basic troubleshooting.Overseeing small maintenance repairs and using organization's work order system for maintenance or improvement requests.Aid in selection, training, developing, motivating, and evaluating employees.Develop employee's knowledge, understanding, and skills to improve performance and expand abilities.Ensure employees remain current with all department and site training requirements.Complete performance reviews for direct reports and review job descriptions on an annual basis.Taking an active role in incident inquiry, investigation, and reporting.Communicate the group's status, data and feedback to management.Other tasks as needed by the company.  qualifications: EDUCATION / EXPERIENCE Education : High School Diploma or equivalent required. Bachelor of Science in Chemistry or Chemical Engineering preferred. Experience : Minimum 7 years of manufacturing experience in fine chemicals and pharmaceutical compounds. Prior experience supervising in a fine chemicals and/or pharmaceutical compounds manufacturing environment preferred. Current knowledge of current OSHA, Employment Law, and cGMP regulations required.Working experience with Continuous Improvement and/or Lean Six Sigma methodologies.Exceptional interpersonal skills.Prior experience supervising in a union environment helpful.Working knowledge of Microsoft Office Suite required. PHYSICAL REQUIREMENTS Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plant.Must be able to sit and/or stand for extended periods.Ability to work effectively under pressure to meet deadlines.Frequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, and listening.Must be able to lift 50 lbs.Ability to wear proper safety equipment when working in the plant.  skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: HPI Production Supervisor Waukegan, IL 24/7 Operation - 1 st shift, but open to work 2 nd shift when required. 12 hour shift - Rotating - 5:30am-5:30pm or 5:30pm-5:30am Example - Work Sun, Off Mon/Tues, Work Wed/Thurs, Off Fri, Sat   location: Waukegan, Illinois job type: Permanent salary: $90,000 - 100,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: JOB SUMMARY The Shift Production Supervisor will be responsible for leading a team of manufacturing operators in a team environment and assisting with the manufacture of pharmaceutical products while following cGMP protocol and ensuring a safe, quality, compliant and cost efficient operation. A collaborative working relationship with other Shift Supervisors, the Production Manager and other key groups to help us maintain a cGMP facility dedicated to providing the highest quality product to our customers. ESSENTIAL DUTIES AND RESPONSIBILITIES Supervise personnel/resources for manufacturing of Bulk Pharmaceutical High Purity Ingredients (HPI) regulated by the Food and Drug Administration (FDA) according to current Good Manufacturing Practices (cGMP) regulations and ICH guidelines in accordance with Quality policy and Standard Operating Procedures (SOPs) to accomplish all departmental goals and objectives while operating in a safe manner and in compliance with all applicable regulations.Understanding all manufacturing systems within the production space, including knowledge of ancillary equipment such as storage and distribution systems, waste neutralization systems, heating/cooling units, vacuum units, etc.Ensure tasks are completed in accordance with approved site procedures, batch records, and protocols.Completes, reviews, and corrects critical documentation including SOP Forms, Batch Records, Logbooks, etc., to ensure completeness and accuracy in compliance with all applicable procedures and ensuring quality documentation under good manufacturing and documentation practices.Ensure all Cleaning and Process validation work is done within allotted timeline.Interface with Supply Chain to ensure adherence to production schedule and the development of said schedule.Coordinate manufacturing needs with other departments and ensure efficient operation of the reactor systems and ancillary production support equipment.Ensure that the production area is maintained, organized and cleaned on a daily basis per SOP's including packaging area.Troubleshooting equipment problems and assisting operators in basic troubleshooting.Overseeing small maintenance repairs and using organization's work order system for maintenance or improvement requests.Aid in selection, training, developing, motivating, and evaluating employees.Develop employee's knowledge, understanding, and skills to improve performance and expand abilities.Ensure employees remain current with all department and site training requirements.Complete performance reviews for direct reports and review job descriptions on an annual basis.Taking an active role in incident inquiry, investigation, and reporting.Communicate the group's status, data and feedback to management.Other tasks as needed by the company.  qualifications: EDUCATION / EXPERIENCE Education : High School Diploma or equivalent required. Bachelor of Science in Chemistry or Chemical Engineering preferred. Experience : Minimum 7 years of manufacturing experience in fine chemicals and pharmaceutical compounds. Prior experience supervising in a fine chemicals and/or pharmaceutical compounds manufacturing environment preferred. Current knowledge of current OSHA, Employment Law, and cGMP regulations required.Working experience with Continuous Improvement and/or Lean Six Sigma methodologies.Exceptional interpersonal skills.Prior experience supervising in a union environment helpful.Working knowledge of Microsoft Office Suite required. PHYSICAL REQUIREMENTS Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plant.Must be able to sit and/or stand for extended periods.Ability to work effectively under pressure to meet deadlines.Frequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, and listening.Must be able to lift 50 lbs.Ability to wear proper safety equipment when working in the plant.  skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • grayslake, illinois
    • permanent
    • $45,000 - $50,000 per year
    Looking for a flexible individual who can work onsite and balance Administrative tasks associated with setting up Trade Show needs and Customer Service/Order Entry & follow up tasks.  Ideal Candidate will be: multi-tasking individual self-motivated possess good communication and interpersonal skills Please send your resume for immediate consideration to Leah.Barrile@randstadusa.com salary: $45,000 - $50,000 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: High` SchoolResponsibilities Processing Orders Ownership of Customer Issues  Communicate effectively and manage the various activities required by marketing team SkillsActive ListeningBasic Computer SkillsCUSTOMER ORDERS/SALESCustomer supportCustomer ServiceBasic Software SkillsClient ServiceCustomer Relationship ManagementQualificationsYears of experience: 3 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Looking for a flexible individual who can work onsite and balance Administrative tasks associated with setting up Trade Show needs and Customer Service/Order Entry & follow up tasks.  Ideal Candidate will be: multi-tasking individual self-motivated possess good communication and interpersonal skills Please send your resume for immediate consideration to Leah.Barrile@randstadusa.com salary: $45,000 - $50,000 per yearshift: Firstwork hours: 8 AM - 4 PMeducation: High` SchoolResponsibilities Processing Orders Ownership of Customer Issues  Communicate effectively and manage the various activities required by marketing team SkillsActive ListeningBasic Computer SkillsCUSTOMER ORDERS/SALESCustomer supportCustomer ServiceBasic Software SkillsClient ServiceCustomer Relationship ManagementQualificationsYears of experience: 3 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • libertyville, illinois
    • permanent
    • $80,000 - $90,000 per year
    job summary: Our Client is looking for an experienced Quality Assurance Engineer to investigate root cause issues, analyse quality data, and lead team members conclusions about non-conformances and driving corrective actions. Ideal candidate will have B.S. in Engineering with 3+ years of quality engineering experience. They will also support have experience with CAD, CREO, and Windchill, while being knowledgeable on continuous improvement, QA Standards and methodologies. Our client provides fantastic benefits and bonuses!  location: Libertyville, Illinois job type: Permanent salary: $80,000 - 90,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Quality Engineer is responsible for investigating root cause issues, analyzing quality data, and leading team members to conclusions - includes investigating non-conformances and driving corrective actions. As assigned, may be responsible for improving incoming material quality, in-process product quality, and outbound product quality. Support the organization in?driving an environment of continuous quality improvement?while maintaining focus?on customer quality. Core?ResponsibilitiesPartner within the business to solve difficult challenges associated with creating and maintaining quality management systems and processes supporting ISO standards.Utilize daily production and monthly global quality data to enact quality improvementsEngage with internal teams (Quality, Production Sourcing, Purchasing) daily to meet Operations plansInfluence the organization to continually improve processes that meet customer/regulatory requirements through maintaining knowledge of best-in-class systems, management tools, and techniques. Champion quality initiatives?and report global quality measurements to key stakeholders Establish production quality requirements, verify quality plans and confirm supplier corrective actions were properly implemented Work with the Supplier Quality Engineer as needed to proactively engage suppliers in order to ensure ongoing quality performance improvement Identify, prioritize and lead production in resolution of existing and potential quality problems As needed, support concurrent engineering efforts by participating in design development projects?by?representing?Quality?Assurance and?our Customers Ensure proper?information flow on quality concerns?to Service Parts, Distributors,?and affiliates Partner with Marketing and Sales?to determine exposure/impact of quality problems?as well as?potential improvements Establish/maintain?effective?systems of internal communications?to all?quality stakeholders Identify, lead and develop production talent to maximize individual, team and organizational effectiveness? Other duties as assigned   qualifications: Experience level: ManagerMinimum 3 years of experienceEducation: Bachelors (required)  skills: Quality (5 years of experience is required)Quality Assurance (3 years of experience is required)Six Sigma (3 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our Client is looking for an experienced Quality Assurance Engineer to investigate root cause issues, analyse quality data, and lead team members conclusions about non-conformances and driving corrective actions. Ideal candidate will have B.S. in Engineering with 3+ years of quality engineering experience. They will also support have experience with CAD, CREO, and Windchill, while being knowledgeable on continuous improvement, QA Standards and methodologies. Our client provides fantastic benefits and bonuses!  location: Libertyville, Illinois job type: Permanent salary: $80,000 - 90,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Quality Engineer is responsible for investigating root cause issues, analyzing quality data, and leading team members to conclusions - includes investigating non-conformances and driving corrective actions. As assigned, may be responsible for improving incoming material quality, in-process product quality, and outbound product quality. Support the organization in?driving an environment of continuous quality improvement?while maintaining focus?on customer quality. Core?ResponsibilitiesPartner within the business to solve difficult challenges associated with creating and maintaining quality management systems and processes supporting ISO standards.Utilize daily production and monthly global quality data to enact quality improvementsEngage with internal teams (Quality, Production Sourcing, Purchasing) daily to meet Operations plansInfluence the organization to continually improve processes that meet customer/regulatory requirements through maintaining knowledge of best-in-class systems, management tools, and techniques. Champion quality initiatives?and report global quality measurements to key stakeholders Establish production quality requirements, verify quality plans and confirm supplier corrective actions were properly implemented Work with the Supplier Quality Engineer as needed to proactively engage suppliers in order to ensure ongoing quality performance improvement Identify, prioritize and lead production in resolution of existing and potential quality problems As needed, support concurrent engineering efforts by participating in design development projects?by?representing?Quality?Assurance and?our Customers Ensure proper?information flow on quality concerns?to Service Parts, Distributors,?and affiliates Partner with Marketing and Sales?to determine exposure/impact of quality problems?as well as?potential improvements Establish/maintain?effective?systems of internal communications?to all?quality stakeholders Identify, lead and develop production talent to maximize individual, team and organizational effectiveness? Other duties as assigned   qualifications: Experience level: ManagerMinimum 3 years of experienceEducation: Bachelors (required)  skills: Quality (5 years of experience is required)Quality Assurance (3 years of experience is required)Six Sigma (3 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • libertyville, illinois
    • permanent
    • $80,000 - $90,000 per year
    job summary: Our Client is looking for an experienced Quality Engineer to investigate root cause issues, analyse quality data, and lead team members conclusions about non-conformances and driving corrective actions. Ideal candidate will have B.S. in Engineering with 3+ years of quality engineering experience. They will also support have experience with CAD, CREO, and Windchill, while being knowledgeable on continuous improvement, QA Standards and methodologies. Client provides fantastic benefits and bonuses!  location: Libertyville, Illinois job type: Permanent salary: $80,000 - 90,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Quality Engineer is responsible for investigating root cause issues, analyzing quality data, and leading team members to conclusions - includes investigating non-conformances and driving corrective actions. As assigned, may be responsible for improving incoming material quality, in-process product quality, and outbound product quality. Support the organization in?driving an environment of continuous quality improvement?while maintaining focus?on customer quality. Core?ResponsibilitiesPartner within the business to solve difficult challenges associated with creating and maintaining quality management systems and processes supporting ISO standards.Utilize daily production and monthly global quality data to enact quality improvementsEngage with internal teams (Quality, Production Sourcing, Purchasing) daily to meet Operations plansInfluence the organization to continually improve processes that meet customer/regulatory requirements through maintaining knowledge of best-in-class systems, management tools, and techniques. Champion quality initiatives?and report global quality measurements to key stakeholders Establish production quality requirements, verify quality plans and confirm supplier corrective actions were properly implemented Work with the Supplier Quality Engineer as needed to proactively engage suppliers in order to ensure ongoing quality performance improvement Identify, prioritize and lead production in resolution of existing and potential quality problems As needed, support concurrent engineering efforts by participating in design development projects?by?representing?Quality?Assurance and?our Customers Ensure proper?information flow on quality concerns?to Service Parts, Distributors,?and affiliates Partner with Marketing and Sales?to determine exposure/impact of quality problems?as well as?potential improvements Establish/maintain?effective?systems of internal communications?to all?quality stakeholders Identify, lead and develop production talent to maximize individual, team and organizational effectiveness? Other duties as assigned   qualifications: Experience level: ManagerMinimum 3 years of experienceEducation: Bachelors (required)  skills: Quality (5 years of experience is required)Quality Assurance (3 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our Client is looking for an experienced Quality Engineer to investigate root cause issues, analyse quality data, and lead team members conclusions about non-conformances and driving corrective actions. Ideal candidate will have B.S. in Engineering with 3+ years of quality engineering experience. They will also support have experience with CAD, CREO, and Windchill, while being knowledgeable on continuous improvement, QA Standards and methodologies. Client provides fantastic benefits and bonuses!  location: Libertyville, Illinois job type: Permanent salary: $80,000 - 90,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: Quality Engineer is responsible for investigating root cause issues, analyzing quality data, and leading team members to conclusions - includes investigating non-conformances and driving corrective actions. As assigned, may be responsible for improving incoming material quality, in-process product quality, and outbound product quality. Support the organization in?driving an environment of continuous quality improvement?while maintaining focus?on customer quality. Core?ResponsibilitiesPartner within the business to solve difficult challenges associated with creating and maintaining quality management systems and processes supporting ISO standards.Utilize daily production and monthly global quality data to enact quality improvementsEngage with internal teams (Quality, Production Sourcing, Purchasing) daily to meet Operations plansInfluence the organization to continually improve processes that meet customer/regulatory requirements through maintaining knowledge of best-in-class systems, management tools, and techniques. Champion quality initiatives?and report global quality measurements to key stakeholders Establish production quality requirements, verify quality plans and confirm supplier corrective actions were properly implemented Work with the Supplier Quality Engineer as needed to proactively engage suppliers in order to ensure ongoing quality performance improvement Identify, prioritize and lead production in resolution of existing and potential quality problems As needed, support concurrent engineering efforts by participating in design development projects?by?representing?Quality?Assurance and?our Customers Ensure proper?information flow on quality concerns?to Service Parts, Distributors,?and affiliates Partner with Marketing and Sales?to determine exposure/impact of quality problems?as well as?potential improvements Establish/maintain?effective?systems of internal communications?to all?quality stakeholders Identify, lead and develop production talent to maximize individual, team and organizational effectiveness? Other duties as assigned   qualifications: Experience level: ManagerMinimum 3 years of experienceEducation: Bachelors (required)  skills: Quality (5 years of experience is required)Quality Assurance (3 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • permanent
    • $75,000 - $80,000 per year
    job summary: Environmental Health & Safety (EHS) Supervisor $80K - some flex on salary 4% yearly bonus 1 st shift / M-F (8am-4:30pm) JOB SUMMARY The Environmental Health and Safety (EHS) Supervisor will assist the EHS Manager in ensuring compliance of all safety, environmental, and health policies and regulations at the company, local, state, and federal levels. The position will assist in identifying, implementing, and maintaining EHS programs in a FDA regulated pharmaceutical manufacturing environment. Key responsibilities include: safety, environmental and chemical regulatory compliance, various safety training, injury reduction, and air emissions/hazardous waste/wastewater management.   location: Waukegan, Illinois job type: Permanent salary: $75,000 - 80,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES Provide EHS guidance and support to ensure compliance with regulatory (OSHA, EPA, IEPA, DOT, etc.) and company requirementsPrepare and submit various EPA/environmental reports, including but not limited to: Tier II Chemical Inventory, Hazardous Waste Report, Air Emission Report, Toxic Release Inventory Report (TRI)Assist the EHS Coordinator with Hazardous Waste Program, including inspections, data tracking, and shipment coordinationAssist EHS Manager with training, new employee safety orientation, incident investigation, and other assigned EHS tasks at the direction of EHS ManagerOversee employee and contractor EHS compliance during normal operations and construction activitiesManagement of the site Safety Inspection Program, including tracking of completionIssue hot work, confined space entry, and other similar permits as necessary Management of Safety Data Sheets (SDS's) and organization of SDS library Assist with site security, including management of visitors and responding to alarmsAssist the EHS Manager with standard operating procedure revisions and updates Perform safety observations at the direction of the EHS ManagerEnsure appropriate tracking and documented closure on all corrective action/audit items, and actively seek to improve compliance Complete Industrial Hygiene Monitoring for various employee exposures, including noise, chemical, and potent compoundsConduct daily activities facility-wide, such as inspections, housekeeping, internal audits, etc.Operate following cGMP regulations and ICH guidelines in accordance with quality policies and Standard Operating ProceduresMaintain a clean, safe, and orderly workplacePerform other duties as assigned  qualifications: QUALIFICATIONS Knowledge of federal, state, and local EHS regulations (OSHA, EPA, IEPA, DOT, etc.)Familiarity with cGMP preferredFamiliarity with environmental reporting requirements preferredAbility to lead safety improvement programs in a plant environmentMust have strong interpersonal skills and be able to interface with all employeesFlexibility to accept new duties as assignedProven ability to work in a team environmentStrong proficiency in Microsoft office applications requiredAble to read, write, and speak technical English EDUCATION / EXPERIENCE Bachelor's Degree in occupational safety and health, environment, or related safety/technical/science field preferredMinimum 3 years of experience as an EHS professional is required, primarily environmental compliance Experience in an FDA-regulated manufacturing environment is preferredExperience in EPA/environmental reporting preferred Professional certification a plusLicensed Waste Treatment Plant Operator and Underground Storage Tank Operator, or ability to become licensed within 1 year after employment  skills: Environmental Sampling Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Environmental Health & Safety (EHS) Supervisor $80K - some flex on salary 4% yearly bonus 1 st shift / M-F (8am-4:30pm) JOB SUMMARY The Environmental Health and Safety (EHS) Supervisor will assist the EHS Manager in ensuring compliance of all safety, environmental, and health policies and regulations at the company, local, state, and federal levels. The position will assist in identifying, implementing, and maintaining EHS programs in a FDA regulated pharmaceutical manufacturing environment. Key responsibilities include: safety, environmental and chemical regulatory compliance, various safety training, injury reduction, and air emissions/hazardous waste/wastewater management.   location: Waukegan, Illinois job type: Permanent salary: $75,000 - 80,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES Provide EHS guidance and support to ensure compliance with regulatory (OSHA, EPA, IEPA, DOT, etc.) and company requirementsPrepare and submit various EPA/environmental reports, including but not limited to: Tier II Chemical Inventory, Hazardous Waste Report, Air Emission Report, Toxic Release Inventory Report (TRI)Assist the EHS Coordinator with Hazardous Waste Program, including inspections, data tracking, and shipment coordinationAssist EHS Manager with training, new employee safety orientation, incident investigation, and other assigned EHS tasks at the direction of EHS ManagerOversee employee and contractor EHS compliance during normal operations and construction activitiesManagement of the site Safety Inspection Program, including tracking of completionIssue hot work, confined space entry, and other similar permits as necessary Management of Safety Data Sheets (SDS's) and organization of SDS library Assist with site security, including management of visitors and responding to alarmsAssist the EHS Manager with standard operating procedure revisions and updates Perform safety observations at the direction of the EHS ManagerEnsure appropriate tracking and documented closure on all corrective action/audit items, and actively seek to improve compliance Complete Industrial Hygiene Monitoring for various employee exposures, including noise, chemical, and potent compoundsConduct daily activities facility-wide, such as inspections, housekeeping, internal audits, etc.Operate following cGMP regulations and ICH guidelines in accordance with quality policies and Standard Operating ProceduresMaintain a clean, safe, and orderly workplacePerform other duties as assigned  qualifications: QUALIFICATIONS Knowledge of federal, state, and local EHS regulations (OSHA, EPA, IEPA, DOT, etc.)Familiarity with cGMP preferredFamiliarity with environmental reporting requirements preferredAbility to lead safety improvement programs in a plant environmentMust have strong interpersonal skills and be able to interface with all employeesFlexibility to accept new duties as assignedProven ability to work in a team environmentStrong proficiency in Microsoft office applications requiredAble to read, write, and speak technical English EDUCATION / EXPERIENCE Bachelor's Degree in occupational safety and health, environment, or related safety/technical/science field preferredMinimum 3 years of experience as an EHS professional is required, primarily environmental compliance Experience in an FDA-regulated manufacturing environment is preferredExperience in EPA/environmental reporting preferred Professional certification a plusLicensed Waste Treatment Plant Operator and Underground Storage Tank Operator, or ability to become licensed within 1 year after employment  skills: Environmental Sampling Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • libertyville, illinois
    • permanent
    • $100,000 - $120,000 per year
    job summary: Our Client is looking for an experienced Supplier Quality Engineer to drive supplier quality assurance through initial supplier survey and working with other teams to confirm part requirements, analyze quality data, etc. Ideal candidate will have B.S. in Engineering with 5+ years of supplier quality engineering experience. If you are a Certified Auditor, that's a plus!!! They will also support purchasing with new and existing supplier assessments, establish communication to quality stakeholders, report on quality issues and preventive actions. Please apply if you have 5+ years of experience in QA/QC supervisor and management capacity, with good oral and written communication skills, and a growing desire to train and move ahead in the company. Company provides fantastic benefits and bonuses!  location: Libertyville, Illinois job type: Permanent salary: $100,000 - 120,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: The Supplier Quality Engineer is responsible to proactively drive supplier quality assurance/control through initial supplier survey/qualification and follow-up confirmations. This position works closely with other teams and applicable groups to confirm part requirements, analyze supplier quality data (i.e. Cpk, capability studies), investigate non-conformances, and ensure adherence to supplier quality expectations.Partner within the business to solve difficult challenges associated with creating and maintaining quality management systems and processes supporting ISO standards.Partner with Engineering, Sourcing and all other applicable groups in product development process.Establish supplier quality requirements, verify quality plans and confirm corrective actions were properly implemented. Conduct supplier audits to drive process standardization and continuous improvements.Develop and implement control plans and specifications; validate supplier quality controls.Strategically lead supplier performance improvement projects in efforts to increase the supplier capability.Travel to supplier location to resolve quality problems.Collaborate with other teams to resolve quality issues.Support Purchasing with new / existing supplier assessments.Establish/maintain?effective?systems of internal communications?to all?quality stakeholders. Report to management on quality issues, trends and preventive actions.   qualifications: Experience level: ManagerMinimum 5 years of experienceEducation: Bachelors (required)  skills: Quality (5 years of experience is required)Supplier Quality (5 years of experience is required)Six Sigma (5 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our Client is looking for an experienced Supplier Quality Engineer to drive supplier quality assurance through initial supplier survey and working with other teams to confirm part requirements, analyze quality data, etc. Ideal candidate will have B.S. in Engineering with 5+ years of supplier quality engineering experience. If you are a Certified Auditor, that's a plus!!! They will also support purchasing with new and existing supplier assessments, establish communication to quality stakeholders, report on quality issues and preventive actions. Please apply if you have 5+ years of experience in QA/QC supervisor and management capacity, with good oral and written communication skills, and a growing desire to train and move ahead in the company. Company provides fantastic benefits and bonuses!  location: Libertyville, Illinois job type: Permanent salary: $100,000 - 120,000 per year work hours: 8am to 5pm education: Bachelors   responsibilities: The Supplier Quality Engineer is responsible to proactively drive supplier quality assurance/control through initial supplier survey/qualification and follow-up confirmations. This position works closely with other teams and applicable groups to confirm part requirements, analyze supplier quality data (i.e. Cpk, capability studies), investigate non-conformances, and ensure adherence to supplier quality expectations.Partner within the business to solve difficult challenges associated with creating and maintaining quality management systems and processes supporting ISO standards.Partner with Engineering, Sourcing and all other applicable groups in product development process.Establish supplier quality requirements, verify quality plans and confirm corrective actions were properly implemented. Conduct supplier audits to drive process standardization and continuous improvements.Develop and implement control plans and specifications; validate supplier quality controls.Strategically lead supplier performance improvement projects in efforts to increase the supplier capability.Travel to supplier location to resolve quality problems.Collaborate with other teams to resolve quality issues.Support Purchasing with new / existing supplier assessments.Establish/maintain?effective?systems of internal communications?to all?quality stakeholders. Report to management on quality issues, trends and preventive actions.   qualifications: Experience level: ManagerMinimum 5 years of experienceEducation: Bachelors (required)  skills: Quality (5 years of experience is required)Supplier Quality (5 years of experience is required)Six Sigma (5 years of experience is required) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • round lake, illinois
    • contract
    • $30 - $37.29 per hour
    job summary: Leader in medical device manufacturing is looking for Engineer in Round Lake, IL for a contract role expected to last 12 months, possible extension, possible temp to perm. This position will effectively design, write and execute engineering studies, direct activities of laboratory technicians, develop detailed project schedules, while working closely with manufacturing plants, Quality, and various scientific/technical groups. Communicate project and task status to project team members, management, and stakeholders on a regular basis.   location: Round Lake, Illinois job type: Contract salary: $30.00 - 37.29 per hour work hours: 8am to 5pm education: Bachelors   responsibilities: Act independently with some supervision to conduct smaller approved projects.Perform basic statistical analysis using Minitab and interpret functional testing resultsContribute to the planning and execution of components of the development process, which apply to product revision or enhancement or a defined piece of a larger project.Ability to manage routine small projects without assistance.Utilize engineering tools to solve straightforward problems (e.g., FMEA, DMAIC Tools, Failure Mode Analysis, Process Modeling, Design of Experiments, Statistical Analysis). Education/Experience: BS in Engineering and 1 - 3 years experience.   qualifications: Experience level: ExperiencedEducation: Bachelors  skills: LaboratoryProfessional Engineer Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Leader in medical device manufacturing is looking for Engineer in Round Lake, IL for a contract role expected to last 12 months, possible extension, possible temp to perm. This position will effectively design, write and execute engineering studies, direct activities of laboratory technicians, develop detailed project schedules, while working closely with manufacturing plants, Quality, and various scientific/technical groups. Communicate project and task status to project team members, management, and stakeholders on a regular basis.   location: Round Lake, Illinois job type: Contract salary: $30.00 - 37.29 per hour work hours: 8am to 5pm education: Bachelors   responsibilities: Act independently with some supervision to conduct smaller approved projects.Perform basic statistical analysis using Minitab and interpret functional testing resultsContribute to the planning and execution of components of the development process, which apply to product revision or enhancement or a defined piece of a larger project.Ability to manage routine small projects without assistance.Utilize engineering tools to solve straightforward problems (e.g., FMEA, DMAIC Tools, Failure Mode Analysis, Process Modeling, Design of Experiments, Statistical Analysis). Education/Experience: BS in Engineering and 1 - 3 years experience.   qualifications: Experience level: ExperiencedEducation: Bachelors  skills: LaboratoryProfessional Engineer Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • permanent
    • $52,000 - $55,000 per year
    job summary: QA Coordinator JOB SUMMARY QA Coordinator is an integral member of the Quality Assurance / Regulatory Affairs department that is responsible for reviewing and approving production batch records and analytical records to meet company and departmental objectives. The Quality Coordinator is the lead and back-up support of the following systems: Batch Record ReviewRaw Material and Finished Product ReleaseAnalytical Data ReviewLaboratory Report ReviewInternal GMP systems auditsTraining Management (SharePoint LMS)Document Control System - Back-upControlled Document Issuance - Back-upCAPA system compliance - Back-up to CAPA Coordinator for system administration Must be able to use site specific Electronic Resource Planning (ERP) systems and other systems to review and approve incoming raw material and finished product documentation and records. The position requires a thorough working knowledge of databases and computer software. Attention to detail is critical for success. Must possess a comprehensive knowledge of global management of change and change control notifications for clients/customers. This knowledge will be used to assess all documents reviewed to ensure compliance with all internal and external requirements. Must possess a comprehensive knowledge of ICH Q7, the industry's cGMP standard and the relation of this guidance to production records.   location: Waukegan, Illinois job type: Permanent salary: $52,000 - 55,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES Operate in accordance and compliance with: Current cGMP regulations and ICH Q7 guidelinesCardinal Rules of Quality, Delivery and Safety Perform all of the duties and responsibilities of Quality Assurance Coordinator. Batch Record Review - Review and approve all applicable GMP records associated with the manufacture and release of Active Pharmaceutical Ingredients, Excipients, Food Additives, and fine chemicals. Batch record review and release of incoming raw materials, intermediates, finished products and cleaning procedures for all Excipient and API business. Working closely with manufacturing to ensure GMP/GDP practices.Analytical data package review as a part of batch record release.Log sheet reviews of all equipment used during product manufacturing.Ensure that manufacturing and laboratory personnel are properly trained for the tasks performed through training record review.Equipment utilized during manufacturing has been properly qualified / calibrated / validated.Data documentation and corrections to documentation are properly executed in compliance with cGMP Good Documentation Practices. Report Review - Participate in the review and approval of various laboratory reports. Method Development and Validation protocols and reports.Stability protocols.Reference standard qualification/requalification reports. Audits - Participate in and lead internal audits of Quality Systems in regard to cGMP. Participate in customer GMP audits of the facility. Review previous audit observations for the area being audited.Obtain / present / explain any data or procedural documents requested by the Auditor(s) associated with position.Identify and summon subject matter experts for assistance when necessary.Participate on the Internal Audit Team by performing system, process or procedural departmental audits according to the established internal audit schedule. 1. SharePoint LMS - Assist in the administration of the training system. Ensure that the necessary personnel updates and documents are added into the system.Enter QA/RA training records into the system.Maintain the accuracy of the data contained within the system. Corrective and Preventive Action (CAPA) - Work in coordination with the CAPA Coordinator in identifying and implementing deviations and investigations as needed to ensure proper compliance to GMP, Quality Agreements, Internal policies and procedures. Other Functions - Perform general administrative duties for the QA/RA department. Cross-train with other functions within QA/RA department. 100% attendance to all Safety and GMP training. Create/revise and review document change requests for SOP's and PBR's.Project team memberInteract and communicate with manufacturing, supply chain, materials management, sales, engineering, process support/R&D, quality control and accounting on a daily basis to ensure awareness and compliance.Correspond with clients in regards to batch record release/review when necessary (i.e. Customer owned products).   qualifications: QUALIFICATIONS A Bachelor's degree or equivalent experience and 2-5 years of experience in a GMP regulated industry. A degree in the Sciences is preferred.Computer skills - Microsoft Office software and databases.Working knowledge of the cGMP regulations (ICH Q7).Motivation and attention to detail are essential.Good observation, organization, prioritization and problem-solving skills.Must display the ability to lead teams and handle project management activities with supervision.Must demonstrate effective communication skills and technical writing ability. PHYSICAL REQUIREMENTS Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plantMust be able to sit and/or stand for extended periodsAbility to work effectively under pressure to meet deadlinesFrequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, listeningMust be able to lift 50 lbs.Ability to wear proper safety equipment when working in plant  skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: QA Coordinator JOB SUMMARY QA Coordinator is an integral member of the Quality Assurance / Regulatory Affairs department that is responsible for reviewing and approving production batch records and analytical records to meet company and departmental objectives. The Quality Coordinator is the lead and back-up support of the following systems: Batch Record ReviewRaw Material and Finished Product ReleaseAnalytical Data ReviewLaboratory Report ReviewInternal GMP systems auditsTraining Management (SharePoint LMS)Document Control System - Back-upControlled Document Issuance - Back-upCAPA system compliance - Back-up to CAPA Coordinator for system administration Must be able to use site specific Electronic Resource Planning (ERP) systems and other systems to review and approve incoming raw material and finished product documentation and records. The position requires a thorough working knowledge of databases and computer software. Attention to detail is critical for success. Must possess a comprehensive knowledge of global management of change and change control notifications for clients/customers. This knowledge will be used to assess all documents reviewed to ensure compliance with all internal and external requirements. Must possess a comprehensive knowledge of ICH Q7, the industry's cGMP standard and the relation of this guidance to production records.   location: Waukegan, Illinois job type: Permanent salary: $52,000 - 55,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES Operate in accordance and compliance with: Current cGMP regulations and ICH Q7 guidelinesCardinal Rules of Quality, Delivery and Safety Perform all of the duties and responsibilities of Quality Assurance Coordinator. Batch Record Review - Review and approve all applicable GMP records associated with the manufacture and release of Active Pharmaceutical Ingredients, Excipients, Food Additives, and fine chemicals. Batch record review and release of incoming raw materials, intermediates, finished products and cleaning procedures for all Excipient and API business. Working closely with manufacturing to ensure GMP/GDP practices.Analytical data package review as a part of batch record release.Log sheet reviews of all equipment used during product manufacturing.Ensure that manufacturing and laboratory personnel are properly trained for the tasks performed through training record review.Equipment utilized during manufacturing has been properly qualified / calibrated / validated.Data documentation and corrections to documentation are properly executed in compliance with cGMP Good Documentation Practices. Report Review - Participate in the review and approval of various laboratory reports. Method Development and Validation protocols and reports.Stability protocols.Reference standard qualification/requalification reports. Audits - Participate in and lead internal audits of Quality Systems in regard to cGMP. Participate in customer GMP audits of the facility. Review previous audit observations for the area being audited.Obtain / present / explain any data or procedural documents requested by the Auditor(s) associated with position.Identify and summon subject matter experts for assistance when necessary.Participate on the Internal Audit Team by performing system, process or procedural departmental audits according to the established internal audit schedule. 1. SharePoint LMS - Assist in the administration of the training system. Ensure that the necessary personnel updates and documents are added into the system.Enter QA/RA training records into the system.Maintain the accuracy of the data contained within the system. Corrective and Preventive Action (CAPA) - Work in coordination with the CAPA Coordinator in identifying and implementing deviations and investigations as needed to ensure proper compliance to GMP, Quality Agreements, Internal policies and procedures. Other Functions - Perform general administrative duties for the QA/RA department. Cross-train with other functions within QA/RA department. 100% attendance to all Safety and GMP training. Create/revise and review document change requests for SOP's and PBR's.Project team memberInteract and communicate with manufacturing, supply chain, materials management, sales, engineering, process support/R&D, quality control and accounting on a daily basis to ensure awareness and compliance.Correspond with clients in regards to batch record release/review when necessary (i.e. Customer owned products).   qualifications: QUALIFICATIONS A Bachelor's degree or equivalent experience and 2-5 years of experience in a GMP regulated industry. A degree in the Sciences is preferred.Computer skills - Microsoft Office software and databases.Working knowledge of the cGMP regulations (ICH Q7).Motivation and attention to detail are essential.Good observation, organization, prioritization and problem-solving skills.Must display the ability to lead teams and handle project management activities with supervision.Must demonstrate effective communication skills and technical writing ability. PHYSICAL REQUIREMENTS Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plantMust be able to sit and/or stand for extended periodsAbility to work effectively under pressure to meet deadlinesFrequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, listeningMust be able to lift 50 lbs.Ability to wear proper safety equipment when working in plant  skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • contract
    • $25 - $31.12 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $25.00 - 31.12 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Plan and execute assigned laboratory tasks utilizing standard procedures and technical understanding of various techniques to complete assigned tasks.Develop protocols for more complex tests or experiments performed with less defined assays and parameters.Apply basic computer skills including word processing, spreadsheets, and instrument related systems.Presents conclusions of defined experiments.Ensures safety and GxP requirements are met when performing tasks.Ensures timely and GxP compliant delivery of high quality precise data  qualifications: BS/BA in Chemistry, Chemical Engineer, Biochemistry, Medical Technology, Biology or related field with 2-5 yrs lab experience (pharmaceutical industry preferred) or Masters Degree.Solid use of analytical instruments including HPLC and chromatography data systems (i.e., Empower).Solid documentation skills, familiarity of GMP, GLP.Able to present findings to larger groups.  skills: HPLC, Chemistry, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $25.00 - 31.12 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Plan and execute assigned laboratory tasks utilizing standard procedures and technical understanding of various techniques to complete assigned tasks.Develop protocols for more complex tests or experiments performed with less defined assays and parameters.Apply basic computer skills including word processing, spreadsheets, and instrument related systems.Presents conclusions of defined experiments.Ensures safety and GxP requirements are met when performing tasks.Ensures timely and GxP compliant delivery of high quality precise data  qualifications: BS/BA in Chemistry, Chemical Engineer, Biochemistry, Medical Technology, Biology or related field with 2-5 yrs lab experience (pharmaceutical industry preferred) or Masters Degree.Solid use of analytical instruments including HPLC and chromatography data systems (i.e., Empower).Solid documentation skills, familiarity of GMP, GLP.Able to present findings to larger groups.  skills: HPLC, Chemistry, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lake bluff, illinois
    • temp to perm
    • $25 per hour
    Ready to take on your next great career opportunity? Do you consider yourself a high-impact professional who understands the shipping and distribution functions front to back, inside and out? If so, you might be the right fit for our client. But we’re also looking for a bona fide change agent who can move the needle on key metrics almost immediately upon arrival. We recognize that may be a significant challenge — but you’ll also find that the rewards, in terms of salary and benefits, are more than commensurate. So if you truly think you’re ready to make an impact and hit the ground running, read more about the role as well as our hiring process. Be sure to apply now, too, because we’re setting up online interviews with qualified candidates shortly. ***Send your resume for immediate consideration to Leah.Barrile@randstadusa.com***salary: $25 - $25 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: No Degree RequiredResponsibilities Schedule all shipments based on finished goods inventory, forecasts, and projected demandAudit and disposition on finished goods overages, and logistics related activitiesCheck-in drivers upon arrival, confirm the load they are picking up, and complete all required paperwork to accompany the shipment and for internal purposes.Find and mark coils diverted in finished goods inventoryWork with the loaders when questions or issues arise to resolveCommunicate with freight carriers/companies to ensure all loads have a scheduled dock appointment, and to support with reschedules and adjustments as needed. Develop strategic relationships with carriers.Communicate and work with the Account Management and commercial teams to help support customer requirements.Work in collaboration with other Operations Coordinator, Logistics Supervisor, and logistics leaders to support freight activityUtilize Comcast, Oracle, and TMSSupport in load tendering and load coverage& dispatch activities Skills OrganizationDecision MakingConcastOracleTMSFlexible to ChangeOral CommunicationAudit - InternalScheduling Qualifications Years of experience: 1 yearExperience level: Experienced Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Ready to take on your next great career opportunity? Do you consider yourself a high-impact professional who understands the shipping and distribution functions front to back, inside and out? If so, you might be the right fit for our client. But we’re also looking for a bona fide change agent who can move the needle on key metrics almost immediately upon arrival. We recognize that may be a significant challenge — but you’ll also find that the rewards, in terms of salary and benefits, are more than commensurate. So if you truly think you’re ready to make an impact and hit the ground running, read more about the role as well as our hiring process. Be sure to apply now, too, because we’re setting up online interviews with qualified candidates shortly. ***Send your resume for immediate consideration to Leah.Barrile@randstadusa.com***salary: $25 - $25 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: No Degree RequiredResponsibilities Schedule all shipments based on finished goods inventory, forecasts, and projected demandAudit and disposition on finished goods overages, and logistics related activitiesCheck-in drivers upon arrival, confirm the load they are picking up, and complete all required paperwork to accompany the shipment and for internal purposes.Find and mark coils diverted in finished goods inventoryWork with the loaders when questions or issues arise to resolveCommunicate with freight carriers/companies to ensure all loads have a scheduled dock appointment, and to support with reschedules and adjustments as needed. Develop strategic relationships with carriers.Communicate and work with the Account Management and commercial teams to help support customer requirements.Work in collaboration with other Operations Coordinator, Logistics Supervisor, and logistics leaders to support freight activityUtilize Comcast, Oracle, and TMSSupport in load tendering and load coverage& dispatch activities Skills OrganizationDecision MakingConcastOracleTMSFlexible to ChangeOral CommunicationAudit - InternalScheduling Qualifications Years of experience: 1 yearExperience level: Experienced Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • libertyville, illinois
    • contract
    • $30 - $33 per hour
    job summary: QC Document Specialist 1 st shift - 8am-4pm (M-F) Libertyville, IL   location: Libertyville, Illinois job type: Contract salary: $30 - 33 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities: · Acts as administrator for Quality computerized systems such as LIMS, Empower, and lab computerized systems including Windows permissions. · Serves as subject matter expert for Quality computerized systems and ensure compliance to regulatory requirements such as 21 CFR Part 11 and Annex 11. · Day-to-day management and continuous improvement of all QC computerized systems/processes. · Plans and leads Quality IT projects, such as LIMS implementation and lab instrument qualification. · Works with Quality, IT, and Validation to support Quality computerized system lifecycle management activities from concept, development, validation, implementation and maintenance to retirement. · Supports a harmonized approach with team members across all network sites for Quality systems. · Authors and reviews protocols, reports, investigations, non-conformance, CAPAs, and other records related to Quality computerized systems. · Monitors Quality computerized systems to ensure compliance to regulatory requirements, such as 21 CFR Part 11, and Annex 11. · Assists with data integrity initiatives as they relate to Quality computerized systems. · Leads periodic reviews of existing computerized systems and identify process improvements coordinating implementation of new processes. · Creates/maintains SOPs and training related to Quality IT systems. · Represent Quality IT during meetings. Communicates and tracks all follow-up items through to completion. · Other related duties as assigned.   qualifications: Requirements: · Bachelor's degree in a Scientific, Biotech, Pharmaceutical or IT field of study with 6 years working in a GxP pharma or biotech environment preferred. · 3 years instrument administration experience preferred. · 3 years' experience with LIMS administration, especially STARLIMS® preferred. · 3 years' experience with chromatography data systems, especially Waters Empower® preferred. · Familiarity with Windows permission settings, network domain, and a general understanding of server architecture. · Prefer familiarity with SQL, Java, or other LIMS programming language. · Experience should include lifecycle management of Quality computerized systems.   skills: LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: QC Document Specialist 1 st shift - 8am-4pm (M-F) Libertyville, IL   location: Libertyville, Illinois job type: Contract salary: $30 - 33 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities: · Acts as administrator for Quality computerized systems such as LIMS, Empower, and lab computerized systems including Windows permissions. · Serves as subject matter expert for Quality computerized systems and ensure compliance to regulatory requirements such as 21 CFR Part 11 and Annex 11. · Day-to-day management and continuous improvement of all QC computerized systems/processes. · Plans and leads Quality IT projects, such as LIMS implementation and lab instrument qualification. · Works with Quality, IT, and Validation to support Quality computerized system lifecycle management activities from concept, development, validation, implementation and maintenance to retirement. · Supports a harmonized approach with team members across all network sites for Quality systems. · Authors and reviews protocols, reports, investigations, non-conformance, CAPAs, and other records related to Quality computerized systems. · Monitors Quality computerized systems to ensure compliance to regulatory requirements, such as 21 CFR Part 11, and Annex 11. · Assists with data integrity initiatives as they relate to Quality computerized systems. · Leads periodic reviews of existing computerized systems and identify process improvements coordinating implementation of new processes. · Creates/maintains SOPs and training related to Quality IT systems. · Represent Quality IT during meetings. Communicates and tracks all follow-up items through to completion. · Other related duties as assigned.   qualifications: Requirements: · Bachelor's degree in a Scientific, Biotech, Pharmaceutical or IT field of study with 6 years working in a GxP pharma or biotech environment preferred. · 3 years instrument administration experience preferred. · 3 years' experience with LIMS administration, especially STARLIMS® preferred. · 3 years' experience with chromatography data systems, especially Waters Empower® preferred. · Familiarity with Windows permission settings, network domain, and a general understanding of server architecture. · Prefer familiarity with SQL, Java, or other LIMS programming language. · Experience should include lifecycle management of Quality computerized systems.   skills: LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • round lake, illinois
    • contract
    • $20 - $24 per hour
    job summary: Leader in medical device manufacturing is looking for Engineering Technician in Round Lake, IL for a contract role expected to last 12 months, possible extension, possible temp to perm. Qualified candidate should have High School diploma or equivalent, AA Degree is preferred, 0-2 years experience. Preferred background in Mechanical Design, Material Science, Design of Experiments, Mold Flow, SPC, Minitab, etc.  location: ROUND LAKE, Illinois job type: Contract salary: $20 - 24 per hour work hours: 8am to 5pm education: High School   responsibilities: Responsible for performing a wide variety of research and/or development laboratory tasks and experiments.May make detailed observations, analyze data and interpret results.Assess results for application, validity and conformance to specifications.Maintain laboratory equipment and inventory levels for laboratory supplies.May write experimental reports, summaries and protocols.May also develop and maintain record keeping for experiment performed.Individual usually is assigned routine assembly and testing portions of projects (e.g. Product performance) May also perform the following functions: requisitioning, defining, initiating, specifying, documenting and training. Skills: Basic computer skills such as word processing, data entry and e-mailBasic science and/or math skillsTeam orientation Include the education and experience that is necessary to perform the job satisfactorily.Ability to manage routine small projects without assistance.Utilize engineering tools to solve straightforward problems Education and Experience: High School diploma or equivalent, AA Degree is preferred, 0-2 years experience.Preferred background in Mechanical Design, Material Science, Design of Experiments, Mold Flow, SPC, Minitab, etc.   qualifications: Experience level: ExperiencedEducation: High School  skills: Mechanical DesignLaboratory Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Leader in medical device manufacturing is looking for Engineering Technician in Round Lake, IL for a contract role expected to last 12 months, possible extension, possible temp to perm. Qualified candidate should have High School diploma or equivalent, AA Degree is preferred, 0-2 years experience. Preferred background in Mechanical Design, Material Science, Design of Experiments, Mold Flow, SPC, Minitab, etc.  location: ROUND LAKE, Illinois job type: Contract salary: $20 - 24 per hour work hours: 8am to 5pm education: High School   responsibilities: Responsible for performing a wide variety of research and/or development laboratory tasks and experiments.May make detailed observations, analyze data and interpret results.Assess results for application, validity and conformance to specifications.Maintain laboratory equipment and inventory levels for laboratory supplies.May write experimental reports, summaries and protocols.May also develop and maintain record keeping for experiment performed.Individual usually is assigned routine assembly and testing portions of projects (e.g. Product performance) May also perform the following functions: requisitioning, defining, initiating, specifying, documenting and training. Skills: Basic computer skills such as word processing, data entry and e-mailBasic science and/or math skillsTeam orientation Include the education and experience that is necessary to perform the job satisfactorily.Ability to manage routine small projects without assistance.Utilize engineering tools to solve straightforward problems Education and Experience: High School diploma or equivalent, AA Degree is preferred, 0-2 years experience.Preferred background in Mechanical Design, Material Science, Design of Experiments, Mold Flow, SPC, Minitab, etc.   qualifications: Experience level: ExperiencedEducation: High School  skills: Mechanical DesignLaboratory Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lake forest, illinois
    • contract
    • $35 - $43.01 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lake Forest, Illinois job type: Contract salary: $35.00 - 43.01 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Assist with the execution of the Quality and Compliance transactional monitoring, including data analysis, development of new transaction monitoring scenarios, and optimization of transaction monitoring processes.Maintain documentation supporting the Quality and Compliance transactional monitoring services, processes, and requirements.Perform root cause analysis and resolve production and data issuesUnderstand how to use data visualization tool to capture key Quality and Compliance metrics and tell the data storySupport and create presentation content that drives the discussion for the quarterly Quality and Compliance meetings.Maintain knowledge of the business risks, systems, and processes to ensure compliance with policies and procedures of established internal and external standards and guidelinesVendor liaison and Relationship Building: Interacts with key monitoring vendor on a daily business to address any platform enhancements and general maintenance.  qualifications: Position requires BS degree in a business or data science related area.3+ years of compliance, internal audit, or business intelligence experienceThe position requires human relations and personal skills necessary to establish and maintain effective working relationships with key vendor partners, team members, and business departments in Legal and OEC.The individual must be detail orientated and understand reporting best practices and the ability to answer the next question via reporting metrics.Experience with excel, power point, and data visualization tools.Ability to communicate concepts and problems in terms that are understandable to all levels of the organizationAn in-depth understanding of the pharmaceutical patient centricity, customer service oriented, and compliance and quality systems is preferred  skills: Quality Assurance, MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lake Forest, Illinois job type: Contract salary: $35.00 - 43.01 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Assist with the execution of the Quality and Compliance transactional monitoring, including data analysis, development of new transaction monitoring scenarios, and optimization of transaction monitoring processes.Maintain documentation supporting the Quality and Compliance transactional monitoring services, processes, and requirements.Perform root cause analysis and resolve production and data issuesUnderstand how to use data visualization tool to capture key Quality and Compliance metrics and tell the data storySupport and create presentation content that drives the discussion for the quarterly Quality and Compliance meetings.Maintain knowledge of the business risks, systems, and processes to ensure compliance with policies and procedures of established internal and external standards and guidelinesVendor liaison and Relationship Building: Interacts with key monitoring vendor on a daily business to address any platform enhancements and general maintenance.  qualifications: Position requires BS degree in a business or data science related area.3+ years of compliance, internal audit, or business intelligence experienceThe position requires human relations and personal skills necessary to establish and maintain effective working relationships with key vendor partners, team members, and business departments in Legal and OEC.The individual must be detail orientated and understand reporting best practices and the ability to answer the next question via reporting metrics.Experience with excel, power point, and data visualization tools.Ability to communicate concepts and problems in terms that are understandable to all levels of the organizationAn in-depth understanding of the pharmaceutical patient centricity, customer service oriented, and compliance and quality systems is preferred  skills: Quality Assurance, MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • libertyville, illinois
    • temporary
    • $20 per hour
    One Day & Short term Project(s) help - Needed IMMEDIATELY 10:45AM - 3:30 PM - other shifts desired as well - Libertyville, Mundelien & Skokie areas Professional Phone Dimeanor/Experience Prompt & Accurate  Reliable Onsite Required Full time and Part Time Projects Available Please send your resume to Leah.Barrile@randstadusa.com for immediate considerationsalary: $20 - $20 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: High` SchoolResponsibilities Professional Phone Dimeanor/Experience Prompt & Accurate  Reliable SkillsGreeting CustomersSwitchboard OperationReceptionist DutiesQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    One Day & Short term Project(s) help - Needed IMMEDIATELY 10:45AM - 3:30 PM - other shifts desired as well - Libertyville, Mundelien & Skokie areas Professional Phone Dimeanor/Experience Prompt & Accurate  Reliable Onsite Required Full time and Part Time Projects Available Please send your resume to Leah.Barrile@randstadusa.com for immediate considerationsalary: $20 - $20 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: High` SchoolResponsibilities Professional Phone Dimeanor/Experience Prompt & Accurate  Reliable SkillsGreeting CustomersSwitchboard OperationReceptionist DutiesQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • waukegan, illinois
    • temp to perm
    • $16 - $18.01 per hour
    Temp to Hire  - We are currently in search of shipping and receiving to work 1st shift in the Waukegan IL  area. Looking for someone who has worked in a production environment.Having worked in a team environment, and having great communication skills, and attendance are required. Primarily work is unloading parts, bringing them to the production areas and then packing parts up to get shipped out. If that sounds good to you, then your next job may be here.    What is in it for you:  Temp to hire Quick start  Competitive pay   If you or anyone you know is looking for a position like this please do not hesitate. Click to apply or call our office at 847-336-3700 or if you want to schedule some time with me directly please click this link to view my calendar: https://calendly.com/joe-kasprzyk/15min or text me at 224-372-0038salary: $16 - $18.01 per hourshift: Firstwork hours: 7 AM - 3:30 PMeducation: No Degree RequiredResponsibilities- Receiving product - Brining product to different work stations  - Using Hoist and lifting equipment  - Packing prodcut to go out  The essential functions of this role include:wearing steel toe shoesworking in a non-temperature controlled environmentmanual lifting up to 50lbsstanding for 8 hours at one timeSkillspickingPackinghoistMaterial HandlingQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Temp to Hire  - We are currently in search of shipping and receiving to work 1st shift in the Waukegan IL  area. Looking for someone who has worked in a production environment.Having worked in a team environment, and having great communication skills, and attendance are required. Primarily work is unloading parts, bringing them to the production areas and then packing parts up to get shipped out. If that sounds good to you, then your next job may be here.    What is in it for you:  Temp to hire Quick start  Competitive pay   If you or anyone you know is looking for a position like this please do not hesitate. Click to apply or call our office at 847-336-3700 or if you want to schedule some time with me directly please click this link to view my calendar: https://calendly.com/joe-kasprzyk/15min or text me at 224-372-0038salary: $16 - $18.01 per hourshift: Firstwork hours: 7 AM - 3:30 PMeducation: No Degree RequiredResponsibilities- Receiving product - Brining product to different work stations  - Using Hoist and lifting equipment  - Packing prodcut to go out  The essential functions of this role include:wearing steel toe shoesworking in a non-temperature controlled environmentmanual lifting up to 50lbsstanding for 8 hours at one timeSkillspickingPackinghoistMaterial HandlingQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • permanent
    • $140,000 - $150,000 per year
    job summary: Our client's location in Waukegan, IL. currently has an opportunity for a Sr. IT Business Systems Analyst - Supply Chain. This SAP Supply Chain Management (SCM) configuration specialist will provides in-depth technical expertise and direction in the development and support of client area application systems/programming requirements and processes. For various size projects and system changes, they oversee and directly contribute to development and implementation of cost effective solutions.   location: Waukegan, Illinois job type: Permanent salary: $140,000 - 150,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Partner with the functional groups to assess business needs utilizing structured interview processes to establish business priorities and document clear requirementsConduct investigation and collaborate with other technical subject matter experts to provide technical advice on adoption or integration of new technologies and corresponding business impact.Develop alternative technical solutions; advise on options, risks, costs and benefits, and impact on other business processes and system priorities.Serve as an SAP functional configuration expert to develop, test and implement significant new solutions. Configure applicable module(s) to design optimal solution.Review, validate and enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.Evaluate SAP notes, new functionality, and upcoming releases for assigned modules.Recommend operational improvements or devise new approaches to technical or process issues to meet business objectives.Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department's operation objectives.Lead in the development of standards and procedures and publish/communicate findings via IOI's, presentations, white papers, etc.Comply with all applicable Corporate and Divisional Policies and procedures. EDUCATION AND EXPERIENCE YOU'LL BRING Required Bachelor's degree in computer science, engineering, business administration or another relevant discipline 8+ years combined experience in Information Technology, Computer Science or Computer engineering in each of the following:8+ years experience in full life-cycle of SAP (ECC) projects8+ years experience of Manufacturing (PP-PI) and Planning module design, configuration, testing, including: Manufacturing (PP-PI): Process Orders, Master data and Integration to related ProcessesPlanning methods and deep knowledge of various strategiesCapacity management and planning board functionalitySound knowledge of interface mapping with legacy/3rd party applications (MES)Handling and Storage Unit Management Experience in facilitating resolution of cross-team integrated topicsExperience and knowledge in integration of SAP with non-SAP systems, including internally-developed and off-the-shelf software Preferred S/4 HANA implementation experience strongly preferredExperience managing individual assignments within large SAP implementations strongly preferredKnowledge of Inventory and Warehouse Management   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: SAP Applications Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our client's location in Waukegan, IL. currently has an opportunity for a Sr. IT Business Systems Analyst - Supply Chain. This SAP Supply Chain Management (SCM) configuration specialist will provides in-depth technical expertise and direction in the development and support of client area application systems/programming requirements and processes. For various size projects and system changes, they oversee and directly contribute to development and implementation of cost effective solutions.   location: Waukegan, Illinois job type: Permanent salary: $140,000 - 150,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Partner with the functional groups to assess business needs utilizing structured interview processes to establish business priorities and document clear requirementsConduct investigation and collaborate with other technical subject matter experts to provide technical advice on adoption or integration of new technologies and corresponding business impact.Develop alternative technical solutions; advise on options, risks, costs and benefits, and impact on other business processes and system priorities.Serve as an SAP functional configuration expert to develop, test and implement significant new solutions. Configure applicable module(s) to design optimal solution.Review, validate and enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.Evaluate SAP notes, new functionality, and upcoming releases for assigned modules.Recommend operational improvements or devise new approaches to technical or process issues to meet business objectives.Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department's operation objectives.Lead in the development of standards and procedures and publish/communicate findings via IOI's, presentations, white papers, etc.Comply with all applicable Corporate and Divisional Policies and procedures. EDUCATION AND EXPERIENCE YOU'LL BRING Required Bachelor's degree in computer science, engineering, business administration or another relevant discipline 8+ years combined experience in Information Technology, Computer Science or Computer engineering in each of the following:8+ years experience in full life-cycle of SAP (ECC) projects8+ years experience of Manufacturing (PP-PI) and Planning module design, configuration, testing, including: Manufacturing (PP-PI): Process Orders, Master data and Integration to related ProcessesPlanning methods and deep knowledge of various strategiesCapacity management and planning board functionalitySound knowledge of interface mapping with legacy/3rd party applications (MES)Handling and Storage Unit Management Experience in facilitating resolution of cross-team integrated topicsExperience and knowledge in integration of SAP with non-SAP systems, including internally-developed and off-the-shelf software Preferred S/4 HANA implementation experience strongly preferredExperience managing individual assignments within large SAP implementations strongly preferredKnowledge of Inventory and Warehouse Management   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: SAP Applications Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • permanent
    • $140,000 - $150,000 per year
    job summary: Our client's location in Waukegan, IL. currently has an opportunity for a Sr. Business Systems Analyst - Procure to Pay. This SAP Procure to Pay (PTP) configuration specialist will provides in-depth technical expertise and direction in the development and support of client area application systems/programming requirements and processes. For various size projects and system changes, they oversee and directly contribute to development and implementation of cost effective solutions.   location: Waukegan, Illinois job type: Permanent salary: $140,000 - 150,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Partner with the functional groups to assess business needs utilizing structured interview processes to establish business priorities and document clear requirementsConduct investigation and collaborate with other technical subject matter experts to provide technical advice on adoption or integration of new technologies and corresponding business impact.Develop alternative technical solutions; advise on options, risks, costs and benefits, and impact on other business processes and system priorities.Serve as an SAP functional configuration expert to develop, test and implement significant new solutions. Configure applicable module(s) to design optimal solution.Review, validate and enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.Evaluate SAP notes, new functionality, and upcoming releases for assigned modules.Recommend operational improvements or devise new approaches to technical or process issues to meet business objectives.Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department's operation objectives.Lead in the development of standards and procedures and publish/communicate findings via IOI's, presentations, white papers, etc.Comply with all applicable Corporate and Divisional Policies and procedures. EDUCATION AND EXPERIENCE YOU'LL BRING Required Bachelor's degree in computer science, engineering, business administration or another relevant discipline 8+ years combined experience in Information Technology, Computer Science or Computer engineering in each of the following: 8+ years experience in full life-cycle of SAP (ECC) projects8+ years of Procure To Pay (PTP) design, configuration, testing, including: Materials Management (MM): Direct and Indirect Procurement (Contracts, Purchase Requisitions/Orders, Goods Receipts, Invoice Receipts, Vendor Master, Source Lists, etc.)Finance-Accounts Payable (FI-AP)Bank integration for paymentsReportingIntegration with other SAP solutions (e.g., MDG, Concur, BW, Ariba, SRM) Experience in facilitating resolution of cross-team integrated topics Experience and knowledge in integration of SAP with non-SAP systems, including internally-developed and off-the-shelf software Preferred S/4 HANA implementation experience strongly preferredExperience managing individual assignments within large SAP implementations strongly preferredAriba and/or Supplier Relationship Management (SRM) configuration   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: SAP Applications Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our client's location in Waukegan, IL. currently has an opportunity for a Sr. Business Systems Analyst - Procure to Pay. This SAP Procure to Pay (PTP) configuration specialist will provides in-depth technical expertise and direction in the development and support of client area application systems/programming requirements and processes. For various size projects and system changes, they oversee and directly contribute to development and implementation of cost effective solutions.   location: Waukegan, Illinois job type: Permanent salary: $140,000 - 150,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Partner with the functional groups to assess business needs utilizing structured interview processes to establish business priorities and document clear requirementsConduct investigation and collaborate with other technical subject matter experts to provide technical advice on adoption or integration of new technologies and corresponding business impact.Develop alternative technical solutions; advise on options, risks, costs and benefits, and impact on other business processes and system priorities.Serve as an SAP functional configuration expert to develop, test and implement significant new solutions. Configure applicable module(s) to design optimal solution.Review, validate and enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.Evaluate SAP notes, new functionality, and upcoming releases for assigned modules.Recommend operational improvements or devise new approaches to technical or process issues to meet business objectives.Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department's operation objectives.Lead in the development of standards and procedures and publish/communicate findings via IOI's, presentations, white papers, etc.Comply with all applicable Corporate and Divisional Policies and procedures. EDUCATION AND EXPERIENCE YOU'LL BRING Required Bachelor's degree in computer science, engineering, business administration or another relevant discipline 8+ years combined experience in Information Technology, Computer Science or Computer engineering in each of the following: 8+ years experience in full life-cycle of SAP (ECC) projects8+ years of Procure To Pay (PTP) design, configuration, testing, including: Materials Management (MM): Direct and Indirect Procurement (Contracts, Purchase Requisitions/Orders, Goods Receipts, Invoice Receipts, Vendor Master, Source Lists, etc.)Finance-Accounts Payable (FI-AP)Bank integration for paymentsReportingIntegration with other SAP solutions (e.g., MDG, Concur, BW, Ariba, SRM) Experience in facilitating resolution of cross-team integrated topics Experience and knowledge in integration of SAP with non-SAP systems, including internally-developed and off-the-shelf software Preferred S/4 HANA implementation experience strongly preferredExperience managing individual assignments within large SAP implementations strongly preferredAriba and/or Supplier Relationship Management (SRM) configuration   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: SAP Applications Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • permanent
    • $140,000 - $150,000 per year
    job summary: Our clien'ts location in Waukegan, IL currently has an opportunity for a Sr. Business Systems Analyst - Record to Report. This SAP Record to Report (RTR) configuration specialist will provide in-depth technical expertise and direction in the development and support of client area application systems/programming requirements and processes. For various size projects and system changes, they oversee and directly contribute to development and implementation of cost effective solutions.   location: Waukegan, Illinois job type: Permanent salary: $140,000 - 150,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Partner with the functional groups to assess business needs utilizing structured interview processes to establish business priorities and document clear requirementsConduct investigation and collaborate with other technical subject matter experts to provide technical advice on adoption or integration of new technologies and corresponding business impact.Develop alternative technical solutions; advise on options, risks, costs and benefits, and impact on other business processes and system priorities.Serve as an SAP functional configuration expert to develop, test and implement significant new solutions. Configure applicable module(s) to design optimal solution.Review, validate and enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.Evaluate SAP notes, new functionality, and upcoming releases for assigned modules.Recommend operational improvements or devise new approaches to technical or process issues to meet business objectives.Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department's operation objectives.Lead in the development of standards and procedures and publish/communicate findings via IOI's, presentations, white papers, etc.Comply with all applicable Corporate and Divisional Policies and procedures. EDUCATION AND EXPERIENCE YOU'LL BRING Required Bachelor's degree in computer science, engineering, business administration or another relevant discipline 8+ years combined experience in Information Technology, Computer Science or Computer engineering in in Record to Report (RTR) functions including: SAP Financial AccountongSAP ControllingSAP TreasurySAP Project Systems Experience in facilitating resolution of cross-team integrated topics Experience and knowledge in integration of SAP with non-SAP systems, including internally-developed and off-the-shelf software Preferred S/4 HANA implementation experience strongly preferredExperience managing individual assignments within large SAP implementations strongly preferred   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: SAP Applications Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Our clien'ts location in Waukegan, IL currently has an opportunity for a Sr. Business Systems Analyst - Record to Report. This SAP Record to Report (RTR) configuration specialist will provide in-depth technical expertise and direction in the development and support of client area application systems/programming requirements and processes. For various size projects and system changes, they oversee and directly contribute to development and implementation of cost effective solutions.   location: Waukegan, Illinois job type: Permanent salary: $140,000 - 150,000 per year work hours: 8am to 4pm education: Bachelors   responsibilities: Partner with the functional groups to assess business needs utilizing structured interview processes to establish business priorities and document clear requirementsConduct investigation and collaborate with other technical subject matter experts to provide technical advice on adoption or integration of new technologies and corresponding business impact.Develop alternative technical solutions; advise on options, risks, costs and benefits, and impact on other business processes and system priorities.Serve as an SAP functional configuration expert to develop, test and implement significant new solutions. Configure applicable module(s) to design optimal solution.Review, validate and enhance design, conduct performance monitoring and capacity planning; install, test and upgrade releases and associated products.Evaluate SAP notes, new functionality, and upcoming releases for assigned modules.Recommend operational improvements or devise new approaches to technical or process issues to meet business objectives.Develop, motivate, and provide direction to technical team in a way that facilitates the creation of a team environment and enables team to fulfill the department's operation objectives.Lead in the development of standards and procedures and publish/communicate findings via IOI's, presentations, white papers, etc.Comply with all applicable Corporate and Divisional Policies and procedures. EDUCATION AND EXPERIENCE YOU'LL BRING Required Bachelor's degree in computer science, engineering, business administration or another relevant discipline 8+ years combined experience in Information Technology, Computer Science or Computer engineering in in Record to Report (RTR) functions including: SAP Financial AccountongSAP ControllingSAP TreasurySAP Project Systems Experience in facilitating resolution of cross-team integrated topics Experience and knowledge in integration of SAP with non-SAP systems, including internally-developed and off-the-shelf software Preferred S/4 HANA implementation experience strongly preferredExperience managing individual assignments within large SAP implementations strongly preferred   qualifications: Experience level: ExperiencedMinimum 8 years of experienceEducation: Bachelors (required)  skills: SAP Applications Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • contract
    • $45 - $51.79 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $45.00 - 51.79 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Must be familiar with ICH and GCP Guidelines.Must demonstrate good interpersonal and organizational communication skills.Determines scope of QC review with the document author and the source documents and/or data required (in addition to utilizing any applicable checklist).Conducts independent quality review of documents by checking against source (documents and/or data) to ensure that the results presented are accurate (emphasis on checking the numbers/data in the text and in-text tables against the final statistical tables, listings, and graphs).Deliver documented quality review comments/checklist to document author through resolution.Ensures QC review documentation from all applicable functional areas is completed and uploaded to the TMF per the established business processes and procedures.Maintains strong knowledge of clinical regulatory documents requiring QC as well as business processes and procedures for these documents. Demonstrates strong attention to detail and a high level of quality, consistency, and accuracy in work effort.Accountable for meeting the main objectives of the assigned projects/roles and responsibilities within established timelines and with an appropriate quality level.Drives the QC of clinical regulatory documents to timely completion.Accountable to Senior Manager, Medical Writing. Exhibits a moderate level of technical competency and requires a low level of counsel and guidance.Mentors and provides guidance/training to less senior MW QC staff as applicable.Expedient escalation of issues to management is essential and may have a direct impact on the ability to meet project timelines.Daily interaction with Medical Writers and/or Medical Writing managers as well as interface/communication with applicable cross-functional areas. Communicates and provides deliverables to Medical Writers, Medical Writing managers, and others as applicable.  qualifications: Bachelor's degree (BA/BS) required.3-5 years relevant pharmaceutical industry experience in medical writing, clinical research, quality, or related area such as regulatory or product support. -Experience in quality review of clinical regulatory documents.-Experience in being flexible with changing workload that requires prioritization and planning to support immediate/urgent business needs.-Proficient experience in use of MS Office (e.g., Word, Excel, Outlook, PowerPoint) and Adobe Acrobat.  skills: Quality control, MS-WORD, MS-EXCEL, MS-Powerpoint, GCP (Good Clinical Practice), ICH Regulations, TMF Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $45.00 - 51.79 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Must be familiar with ICH and GCP Guidelines.Must demonstrate good interpersonal and organizational communication skills.Determines scope of QC review with the document author and the source documents and/or data required (in addition to utilizing any applicable checklist).Conducts independent quality review of documents by checking against source (documents and/or data) to ensure that the results presented are accurate (emphasis on checking the numbers/data in the text and in-text tables against the final statistical tables, listings, and graphs).Deliver documented quality review comments/checklist to document author through resolution.Ensures QC review documentation from all applicable functional areas is completed and uploaded to the TMF per the established business processes and procedures.Maintains strong knowledge of clinical regulatory documents requiring QC as well as business processes and procedures for these documents. Demonstrates strong attention to detail and a high level of quality, consistency, and accuracy in work effort.Accountable for meeting the main objectives of the assigned projects/roles and responsibilities within established timelines and with an appropriate quality level.Drives the QC of clinical regulatory documents to timely completion.Accountable to Senior Manager, Medical Writing. Exhibits a moderate level of technical competency and requires a low level of counsel and guidance.Mentors and provides guidance/training to less senior MW QC staff as applicable.Expedient escalation of issues to management is essential and may have a direct impact on the ability to meet project timelines.Daily interaction with Medical Writers and/or Medical Writing managers as well as interface/communication with applicable cross-functional areas. Communicates and provides deliverables to Medical Writers, Medical Writing managers, and others as applicable.  qualifications: Bachelor's degree (BA/BS) required.3-5 years relevant pharmaceutical industry experience in medical writing, clinical research, quality, or related area such as regulatory or product support. -Experience in quality review of clinical regulatory documents.-Experience in being flexible with changing workload that requires prioritization and planning to support immediate/urgent business needs.-Proficient experience in use of MS Office (e.g., Word, Excel, Outlook, PowerPoint) and Adobe Acrobat.  skills: Quality control, MS-WORD, MS-EXCEL, MS-Powerpoint, GCP (Good Clinical Practice), ICH Regulations, TMF Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • libertyville, illinois
    • temporary
    • $16 - $16.50 per hour
    We are seeking motivated individuals who have great organizational skills and are attentive to detail. This is a contract production position where you will be helping pull pallets, sort cartons/products by color and seriel numbers using an RF Scanner. This is a great opportunity to get a jump start on your career in the Manufacturing industry. There are 1st and 2nd shifts available, all 8 hour shifts Monday-Friday. Pay starts at $16/hr. If this sounds like a job for you, don't wait and APPLY TODAY!  What's in it for you? Consistant hours each week Weekly Pay Growth possiblitlies Great starting pay at $16+/hr  No prior experience required Let us know if you or anyone you know is interested! Text "PRODUCTION" to 224-381-0762 or call us directly at 847-336-3700  salary: $16 - $16.5 per hourshift: Firstwork hours: 2 PM - 11:30 PMeducation: High` SchoolResponsibilities Pull pallets Indentify cartons by seriel #'s using an RF Scanner Scan and sort product based on Color 30 lb lifting Kitting The essential functions of this role include:manual lifting up to 30lbsSkillsSortingRF ScannerKittingPull PalletsAttention to DetailQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    We are seeking motivated individuals who have great organizational skills and are attentive to detail. This is a contract production position where you will be helping pull pallets, sort cartons/products by color and seriel numbers using an RF Scanner. This is a great opportunity to get a jump start on your career in the Manufacturing industry. There are 1st and 2nd shifts available, all 8 hour shifts Monday-Friday. Pay starts at $16/hr. If this sounds like a job for you, don't wait and APPLY TODAY!  What's in it for you? Consistant hours each week Weekly Pay Growth possiblitlies Great starting pay at $16+/hr  No prior experience required Let us know if you or anyone you know is interested! Text "PRODUCTION" to 224-381-0762 or call us directly at 847-336-3700  salary: $16 - $16.5 per hourshift: Firstwork hours: 2 PM - 11:30 PMeducation: High` SchoolResponsibilities Pull pallets Indentify cartons by seriel #'s using an RF Scanner Scan and sort product based on Color 30 lb lifting Kitting The essential functions of this role include:manual lifting up to 30lbsSkillsSortingRF ScannerKittingPull PalletsAttention to DetailQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • round lake, illinois
    • contract
    • $35 - $40.27 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A longtime partner who prides itself on being a leader in many different practical manufacturing processes to better serve the entire population is renowned for pioneering new treatments for renal diseases, immune disorders, and more; the focus is on patient care. If you're looking to be a part of an impactful team, you won't be disappointed! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Round Lake, Illinois job type: Contract salary: $35.00 - 40.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Execute analytical testing following written test procedures and study protocols, document results per GXP regulations, and review data for accuracy and completeness.Apply analytical separation and detection techniques for complex impurity identification/quantification.Execute method validation and transfer studies.Assess the technical feasibility of complex research and design concepts.Contribute to the analytical problem-solving efforts to meet urgent business needs.Collaborate with other functions such as project management, regulatory, formulation, engineering, manufacturing, and quality control in project teams.Collaborate with Company external partners to ensure successful execution of analytical testing and study designs.Develop knowledge of relevant QSR and other regulatory requirements related to R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities.Develop knowledge and understanding of cGxP and related regulations and guidance.Maintain focus on meeting both external and internal customer expectations.  qualifications: Bachelor's degree in relevant scientific discipline (chemistry, pharmaceutical sciences) with 3-5 years' experience or Master's degree with 1-3 years' experience or PhD with 0-3 years' experience.Familiar with GC/MS and/or LC/MS analysis.Familiarity with analytical method development, validation, and transfer in pharmaceutical regulated laboratories is a plus.Awareness of ICH, USP guidelines and cGxP regulations.Familiarity and hands-on experience with HPLC, GC, UV, MassHunter and other analytical instruments and software is a plus.Ability to learn quickly and to solve problems in a timely manner using analytical chemistry skills.Possess relevant writing and computer skills.Ability to design experiments and draw meaningful conclusions from lab data.Quality oriented.Ability to adapt to changes and to work in a team environment.  skills: HPLC, MS-WORD, MS-EXCEL, MS-Powerpoint, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A longtime partner who prides itself on being a leader in many different practical manufacturing processes to better serve the entire population is renowned for pioneering new treatments for renal diseases, immune disorders, and more; the focus is on patient care. If you're looking to be a part of an impactful team, you won't be disappointed! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Round Lake, Illinois job type: Contract salary: $35.00 - 40.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Execute analytical testing following written test procedures and study protocols, document results per GXP regulations, and review data for accuracy and completeness.Apply analytical separation and detection techniques for complex impurity identification/quantification.Execute method validation and transfer studies.Assess the technical feasibility of complex research and design concepts.Contribute to the analytical problem-solving efforts to meet urgent business needs.Collaborate with other functions such as project management, regulatory, formulation, engineering, manufacturing, and quality control in project teams.Collaborate with Company external partners to ensure successful execution of analytical testing and study designs.Develop knowledge of relevant QSR and other regulatory requirements related to R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities.Develop knowledge and understanding of cGxP and related regulations and guidance.Maintain focus on meeting both external and internal customer expectations.  qualifications: Bachelor's degree in relevant scientific discipline (chemistry, pharmaceutical sciences) with 3-5 years' experience or Master's degree with 1-3 years' experience or PhD with 0-3 years' experience.Familiar with GC/MS and/or LC/MS analysis.Familiarity with analytical method development, validation, and transfer in pharmaceutical regulated laboratories is a plus.Awareness of ICH, USP guidelines and cGxP regulations.Familiarity and hands-on experience with HPLC, GC, UV, MassHunter and other analytical instruments and software is a plus.Ability to learn quickly and to solve problems in a timely manner using analytical chemistry skills.Possess relevant writing and computer skills.Ability to design experiments and draw meaningful conclusions from lab data.Quality oriented.Ability to adapt to changes and to work in a team environment.  skills: HPLC, MS-WORD, MS-EXCEL, MS-Powerpoint, GLP (Good Laboratory Practice), GCP (Good Clinical Practice), ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north chicago, illinois
    • contract
    • $40 - $46.22 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $40.00 - 46.22 per hour work hours: 8 to 4 education: High School   responsibilities: Responsible for performing routine testing on incoming materials in accordance with approved specifications and procedures.Disposition incoming material for use in manufacturing.Maintains certification in assigned job responsibilities and completes training on-time.Participates in complaint handling, failure investigations, and CAPA documentation.Understands, implements, and maintains the quality policy and ensures compliance to site level policies and procedures.Develops knowledge of products and technologies. Interacts on a necessary basis with internal and external support groups to perform core skills.Participates in team activities and area metric tracking.Responsible for supporting Operations efforts in meeting established production schedule.Reports problems in a timely and accurate manner.Seeks additional guidance or advice when problem is beyond scope of training or knowledge.  qualifications: High School Diploma required; Bachelors degree preferred.Good understanding of basic math.Good clerical skills is required.4+ years of overall work experienceComputer skills proficiency including word processing, spreadsheets, instrumentation related and Company network systems.Previous experience in Quality Assurance2+ Experience in a manufacturing/finishing environment is desired.Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.Have an understanding of material/product traceability and Device History Records  skills: Quality Assurance, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Chicago, Illinois job type: Contract salary: $40.00 - 46.22 per hour work hours: 8 to 4 education: High School   responsibilities: Responsible for performing routine testing on incoming materials in accordance with approved specifications and procedures.Disposition incoming material for use in manufacturing.Maintains certification in assigned job responsibilities and completes training on-time.Participates in complaint handling, failure investigations, and CAPA documentation.Understands, implements, and maintains the quality policy and ensures compliance to site level policies and procedures.Develops knowledge of products and technologies. Interacts on a necessary basis with internal and external support groups to perform core skills.Participates in team activities and area metric tracking.Responsible for supporting Operations efforts in meeting established production schedule.Reports problems in a timely and accurate manner.Seeks additional guidance or advice when problem is beyond scope of training or knowledge.  qualifications: High School Diploma required; Bachelors degree preferred.Good understanding of basic math.Good clerical skills is required.4+ years of overall work experienceComputer skills proficiency including word processing, spreadsheets, instrumentation related and Company network systems.Previous experience in Quality Assurance2+ Experience in a manufacturing/finishing environment is desired.Previous knowledge of GMP regulations and standards affecting pharmaceutical products is desired.Have an understanding of material/product traceability and Device History Records  skills: Quality Assurance, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
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