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15 jobs found in melrose park, illinois

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    • lake zurich, illinois
    • contract
    • $20 - $25.25 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Lake Zurich, Illinois job type: Contract salary: $20.00 - 25.25 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: Proofreads label copy for instrument manuals and device labels; verifies dimensional accuracy and proper formatting, spelling, and punctuation per established style guides.Ability to check and verify bar codes and H IBC bar codesCompletes additional tasks as assigned by the Manager, Technical Manual Writer and/or Sr. Labeling Proofreader.   qualifications: Must be detail-oriented, task-focused, and adaptable to frequent shifts in priorities.Must be cooperative and work well on a team.Ability to operate independently and effectively under short timelines.Effective oral and written communication skills.Experience using an electronic document management system is preferred.Proficient in Word, Excel, Adobe Acrobat Standard/Pro/DC, Microsoft Outlook  skills: MS-WORD, MS-EXCEL 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 find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Lake Zurich, Illinois job type: Contract salary: $20.00 - 25.25 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: Proofreads label copy for instrument manuals and device labels; verifies dimensional accuracy and proper formatting, spelling, and punctuation per established style guides.Ability to check and verify bar codes and H IBC bar codesCompletes additional tasks as assigned by the Manager, Technical Manual Writer and/or Sr. Labeling Proofreader.   qualifications: Must be detail-oriented, task-focused, and adaptable to frequent shifts in priorities.Must be cooperative and work well on a team.Ability to operate independently and effectively under short timelines.Effective oral and written communication skills.Experience using an electronic document management system is preferred.Proficient in Word, Excel, Adobe Acrobat Standard/Pro/DC, Microsoft Outlook  skills: MS-WORD, MS-EXCEL 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.
    • melrose park, illinois
    • contract
    • $19.08 per hour
    job summary: Randstad is the #1 HR Services Company in the World and we are sourcing for a Quality Control Technician in the suburbs of Chicago, IL. The Quality Control Technician is responsible for performing standardized qualitative and quantitative tests on work-in-process and finished products to ensure compliance with company and/or customer quality standards. This is a contract role and can start immediately.   location: Melrose Park, Illinois job type: Contract work hours: 7 to 3 education: High School   responsibilities: Responsibilities: Make batch adjustments to meet specification.Fill out all documents as necessary to support batching operation.Identify potential problems and correct the situation or notify supervisor.Conduct organoleptic and analytical tests at various stages of compounding and packaging to ensure compliance with standards. May include the use of pH meters, CarboQC, Titrator, and other instrumentation.Monitor elements of HARPC program by conducting RPC checks at prescribed frequencies.Submit samples for microbiological testing, maintains test results, and calculates batch adjustments for certain products.Approve batches for packaging and conforming finished product for shipment and places non-conforming product on hold for further analysis.Make corresponding inventory movements in SAP.File and maintain retained samples.Calibrate, clean, and maintain laboratory equipment and instrumentation.Prepare reagents and solutions for use in testing.Observes conditions and practices in compounding, packaging, and finished goods storage areas, making recommendations for improvement. Perform other job related duties, as assigned by supervisor/manager  qualifications: Requirements: Ability to communicate effectively in order to comprehend standard operating procedures and departmental processes.Self-starter and good decision making skills.Ability to manage personal safety and environmental concerns throughout production environment.Ability to stand, push, pull, stoop, bend, climb, and walk up/down steps repeatedly throughout duration of shift.General PC competencies and familiarity with Microsoft Office.Ability to multi-task to meet production demands.High school diploma or general equivalency diploma (GED). Can be waived for internal candidates.3 years of related Quality Control experience in a manufacturing environment (preferred)Ability to multi-task and manage time effectivelyExperience in a high speed food manufacturing environment (preferred)Ability to stand for duration of shift  skills: Quality control, SOP, Quality Assurance, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), 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: Randstad is the #1 HR Services Company in the World and we are sourcing for a Quality Control Technician in the suburbs of Chicago, IL. The Quality Control Technician is responsible for performing standardized qualitative and quantitative tests on work-in-process and finished products to ensure compliance with company and/or customer quality standards. This is a contract role and can start immediately.   location: Melrose Park, Illinois job type: Contract work hours: 7 to 3 education: High School   responsibilities: Responsibilities: Make batch adjustments to meet specification.Fill out all documents as necessary to support batching operation.Identify potential problems and correct the situation or notify supervisor.Conduct organoleptic and analytical tests at various stages of compounding and packaging to ensure compliance with standards. May include the use of pH meters, CarboQC, Titrator, and other instrumentation.Monitor elements of HARPC program by conducting RPC checks at prescribed frequencies.Submit samples for microbiological testing, maintains test results, and calculates batch adjustments for certain products.Approve batches for packaging and conforming finished product for shipment and places non-conforming product on hold for further analysis.Make corresponding inventory movements in SAP.File and maintain retained samples.Calibrate, clean, and maintain laboratory equipment and instrumentation.Prepare reagents and solutions for use in testing.Observes conditions and practices in compounding, packaging, and finished goods storage areas, making recommendations for improvement. Perform other job related duties, as assigned by supervisor/manager  qualifications: Requirements: Ability to communicate effectively in order to comprehend standard operating procedures and departmental processes.Self-starter and good decision making skills.Ability to manage personal safety and environmental concerns throughout production environment.Ability to stand, push, pull, stoop, bend, climb, and walk up/down steps repeatedly throughout duration of shift.General PC competencies and familiarity with Microsoft Office.Ability to multi-task to meet production demands.High school diploma or general equivalency diploma (GED). Can be waived for internal candidates.3 years of related Quality Control experience in a manufacturing environment (preferred)Ability to multi-task and manage time effectivelyExperience in a high speed food manufacturing environment (preferred)Ability to stand for duration of shift  skills: Quality control, SOP, Quality Assurance, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), 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.
    • melrose park, illinois
    • contract
    • $19.08 per hour
    job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a Quality Control Technician in the suburbs of Chicago, IL. The Quality Control Technician is responsible for performing standardized qualitative and quantitative tests on work-in-process and finished products to ensure compliance with company and/or customer quality standards. This is a contract role and can start immediately.   location: Melrose Park, Illinois job type: Contract work hours: 11 to 7 education: High School   responsibilities: Responsibilities: Make batch adjustments to meet specification.Fill out all documents as necessary to support batching operation.Identify potential problems and correct the situation or notify supervisor.Conduct organoleptic and analytical tests at various stages of compounding and packaging to ensure compliance with standards. May include the use of pH meters, CarboQC, Titrator, and other instrumentation.Monitor elements of HARPC program by conducting RPC checks at prescribed frequencies.Submit samples for microbiological testing, maintains test results, and calculates batch adjustments for certain products.Approve batches for packaging and conforming finished product for shipment and places non-conforming product on hold for further analysis.Make corresponding inventory movements in SAP.File and maintain retained samples.Calibrate, clean, and maintain laboratory equipment and instrumentation.Prepare reagents and solutions for use in testing.Observes conditions and practices in compounding, packaging, and finished goods storage areas, making recommendations for improvement. Perform other job related duties, as assigned by supervisor/manager  qualifications: Requirements: Ability to communicate effectively in order to comprehend standard operating procedures and departmental processes.Self-starter and good decision making skills.Ability to manage personal safety and environmental concerns throughout production environment.Ability to stand, push, pull, stoop, bend, climb, and walk up/down steps repeatedly throughout duration of shift.General PC competencies and familiarity with Microsoft Office.Ability to multi-task to meet production demands.High school diploma or general equivalency diploma (GED). Can be waived for internal candidates.3 years of related Quality Control experience in a manufacturing environment (preferred)Ability to multi-task and manage time effectivelyExperience in a high speed food manufacturing environment (preferred)Ability to stand for duration of shift  skills: Quality control, SOP, Quality Assurance, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), 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: Randstad is the #1 HR Services Company in the world and we are sourcing for a Quality Control Technician in the suburbs of Chicago, IL. The Quality Control Technician is responsible for performing standardized qualitative and quantitative tests on work-in-process and finished products to ensure compliance with company and/or customer quality standards. This is a contract role and can start immediately.   location: Melrose Park, Illinois job type: Contract work hours: 11 to 7 education: High School   responsibilities: Responsibilities: Make batch adjustments to meet specification.Fill out all documents as necessary to support batching operation.Identify potential problems and correct the situation or notify supervisor.Conduct organoleptic and analytical tests at various stages of compounding and packaging to ensure compliance with standards. May include the use of pH meters, CarboQC, Titrator, and other instrumentation.Monitor elements of HARPC program by conducting RPC checks at prescribed frequencies.Submit samples for microbiological testing, maintains test results, and calculates batch adjustments for certain products.Approve batches for packaging and conforming finished product for shipment and places non-conforming product on hold for further analysis.Make corresponding inventory movements in SAP.File and maintain retained samples.Calibrate, clean, and maintain laboratory equipment and instrumentation.Prepare reagents and solutions for use in testing.Observes conditions and practices in compounding, packaging, and finished goods storage areas, making recommendations for improvement. Perform other job related duties, as assigned by supervisor/manager  qualifications: Requirements: Ability to communicate effectively in order to comprehend standard operating procedures and departmental processes.Self-starter and good decision making skills.Ability to manage personal safety and environmental concerns throughout production environment.Ability to stand, push, pull, stoop, bend, climb, and walk up/down steps repeatedly throughout duration of shift.General PC competencies and familiarity with Microsoft Office.Ability to multi-task to meet production demands.High school diploma or general equivalency diploma (GED). Can be waived for internal candidates.3 years of related Quality Control experience in a manufacturing environment (preferred)Ability to multi-task and manage time effectivelyExperience in a high speed food manufacturing environment (preferred)Ability to stand for duration of shift  skills: Quality control, SOP, Quality Assurance, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), 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.
    • deerfield, illinois
    • contract
    • $45 - $54.07 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: Deerfield, Illinois job type: Contract salary: $45.00 - 54.07 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support global product UDI regulatory compliance throughout the product lifecycle: Responsible for aligning with internal requirements and accountable for managing accurate UDI medical device data entered in regulated UDI databases, enabling compliance with UDI regulations in all appropriate global markets (e.g., USA, China, Europe, South Korea, Saudi Arabia)Collaborate with data management professionals, UDI data owners, and sustaining engineering resources to capture, process, and maintain UDI data in internal and external systemsRepresent on internal teams, collaborating on process and system development, testing, and validationEffectively communicate with all internal stakeholders (e.g., R&D, manufacturing etc.) to enable UDI compliant solution implementation and maintenanceEngage with Global Business Unit Regulatory teams and Regional Regulatory teams to ensure regulatory activities are in alignment with business requirements Deliver regulatory support, as assigned: Maintain compliance with regulations (21 CFR 820), standards (ISO 13485), MDR and the Company Corporate Quality ManualWork closely with product development, clinical, and marketing teams to support alignment between required information for new product submissions, labeling, and UDI database entries, providing regulatory input to project teams as required (Example: DHF remediation, labeling guideline)Contribute to document management and control, including document review, approval, archiving, maintenance of document lists, and working with other functional groups on development of new processes or procedures related to UDITimely and actively support to conclusion all associated query responses   qualifications: Required education: Bachelor's degree in a related medical, science, engineering, information technology (IT) or regulatory discipline Required experience: Minimum of 5 years in RA or related healthcare environment, minimum 2 years' experience with medical devicesPrefer experience with UDI and/or international regulatory submissions   skills: GCP (Good Clinical Practice), Regulatory Briefing Documents, Submissions 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: Deerfield, Illinois job type: Contract salary: $45.00 - 54.07 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support global product UDI regulatory compliance throughout the product lifecycle: Responsible for aligning with internal requirements and accountable for managing accurate UDI medical device data entered in regulated UDI databases, enabling compliance with UDI regulations in all appropriate global markets (e.g., USA, China, Europe, South Korea, Saudi Arabia)Collaborate with data management professionals, UDI data owners, and sustaining engineering resources to capture, process, and maintain UDI data in internal and external systemsRepresent on internal teams, collaborating on process and system development, testing, and validationEffectively communicate with all internal stakeholders (e.g., R&D, manufacturing etc.) to enable UDI compliant solution implementation and maintenanceEngage with Global Business Unit Regulatory teams and Regional Regulatory teams to ensure regulatory activities are in alignment with business requirements Deliver regulatory support, as assigned: Maintain compliance with regulations (21 CFR 820), standards (ISO 13485), MDR and the Company Corporate Quality ManualWork closely with product development, clinical, and marketing teams to support alignment between required information for new product submissions, labeling, and UDI database entries, providing regulatory input to project teams as required (Example: DHF remediation, labeling guideline)Contribute to document management and control, including document review, approval, archiving, maintenance of document lists, and working with other functional groups on development of new processes or procedures related to UDITimely and actively support to conclusion all associated query responses   qualifications: Required education: Bachelor's degree in a related medical, science, engineering, information technology (IT) or regulatory discipline Required experience: Minimum of 5 years in RA or related healthcare environment, minimum 2 years' experience with medical devicesPrefer experience with UDI and/or international regulatory submissions   skills: GCP (Good Clinical Practice), Regulatory Briefing Documents, Submissions 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.
    • la grange, illinois
    • temp to perm
    • $19 - $20 per hour
    job summary: Quality/Chemical Coordinator 1 st Shift - 7:30am - 4pm Countryside We will be looking for a Quality/Chemical Coordinator for our quality team. The right candidate will have quality control experience, excellent computer / typing skills, be efficient/responsive and have attention to detail. They will be supporting the plant in the coordination of raw material submittals and releases for the site. Must be from Pharma, Personal Care, Chemical or Food Prefer an Associate Degree - but will take experience rather than having an AS degree   location: La Grange, Illinois job type: Temporary salary: $19 - 20 per hour work hours: 7 to 3 education: High School   responsibilities: Incoming raw material quality representative that coordinates their testing and release   qualifications: High School diploma; preferably Associates Degree in a technical field. 1-2 years Quality team experience in manufacturingKnowledge of cGMPsGood Computer and Communication SkillsFluent in English (reading & speaking)Cooperative and focusedReliable Attendance  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. 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: Quality/Chemical Coordinator 1 st Shift - 7:30am - 4pm Countryside We will be looking for a Quality/Chemical Coordinator for our quality team. The right candidate will have quality control experience, excellent computer / typing skills, be efficient/responsive and have attention to detail. They will be supporting the plant in the coordination of raw material submittals and releases for the site. Must be from Pharma, Personal Care, Chemical or Food Prefer an Associate Degree - but will take experience rather than having an AS degree   location: La Grange, Illinois job type: Temporary salary: $19 - 20 per hour work hours: 7 to 3 education: High School   responsibilities: Incoming raw material quality representative that coordinates their testing and release   qualifications: High School diploma; preferably Associates Degree in a technical field. 1-2 years Quality team experience in manufacturingKnowledge of cGMPsGood Computer and Communication SkillsFluent in English (reading & speaking)Cooperative and focusedReliable Attendance  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. 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.
    • northbrook, illinois
    • contract
    • $30 - $38 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. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now! 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: Northbrook, Illinois job type: Contract salary: $30 - 38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Function as the Quality Document (QD) Administrator responsible for reviewing new or revised Quality Documents for compliance to established standards.Ensure all Quality Documents meet required standards before processing documents in the Company Electronic Document Management System (EDMS) workflows.Ensure impacted stakeholders are involved in the review of new and revised Quality Documents.Deliver effective communication of requirements and standards to Authors of Quality Documents as well as to the Users of the Company EDMS.Support the development, review, and delivery of training materials to provide to new users of the EDMS system.Provide guidance on proper methods for writing SOPs and other Quality Documents to meet standards.Support Document Management / Document Control initiatives that lead to process improvements.Respond to email inquiries and user support questions.Support EDMS end-users on document retrieval for superseded and obsolete documents as well as completing requests for uploading documents and related translations into the EDMS.Support other electronic processes managed by the Document Management Group.  qualifications: REQUIRED SKILLS: Bachelor of Arts/ Bachelor of Science degree BS/BA.2 - 5 years working experience in the pharmaceutical industry within QA and Document Management.Skills and Competencies: Strong interpersonal skills and multi-cultural /intercultural awareness, able to negotiate and build consensus for plans and priorities and able to develop effective relationships through collaboration.Excellent oral and written communication.Ability to work independently, multitask and shift workload according to department/team priorities.Strong planning and organizational skills and experience managing and delivering on multiple priorities in a timely manner.Ability to demonstrate critical thinking while analyzing / resolving issues and improving processes.Proficiency in Microsoft Office (e.g., Word, Excel, PowerPoint) and PDF editor software (e.g., Adobe Professional, Foxit).High attention to detail. PREFERRED SKILLS: Experience processing documents within an EDMS (e.g., Veeva Vault Quality, Master Control).Ability to see the big picture regarding overall process.Ability to demonstrate critical thinking while analyzing / resolving issues and improving processesDemonstrated ability to follow-up on open action itemsExcellent verbal and written communication skills within a global environment.Ability to work independently, multitask and shift workload according to department/team priorities.   skills: Accounts Receivable, 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. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now! 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: Northbrook, Illinois job type: Contract salary: $30 - 38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Function as the Quality Document (QD) Administrator responsible for reviewing new or revised Quality Documents for compliance to established standards.Ensure all Quality Documents meet required standards before processing documents in the Company Electronic Document Management System (EDMS) workflows.Ensure impacted stakeholders are involved in the review of new and revised Quality Documents.Deliver effective communication of requirements and standards to Authors of Quality Documents as well as to the Users of the Company EDMS.Support the development, review, and delivery of training materials to provide to new users of the EDMS system.Provide guidance on proper methods for writing SOPs and other Quality Documents to meet standards.Support Document Management / Document Control initiatives that lead to process improvements.Respond to email inquiries and user support questions.Support EDMS end-users on document retrieval for superseded and obsolete documents as well as completing requests for uploading documents and related translations into the EDMS.Support other electronic processes managed by the Document Management Group.  qualifications: REQUIRED SKILLS: Bachelor of Arts/ Bachelor of Science degree BS/BA.2 - 5 years working experience in the pharmaceutical industry within QA and Document Management.Skills and Competencies: Strong interpersonal skills and multi-cultural /intercultural awareness, able to negotiate and build consensus for plans and priorities and able to develop effective relationships through collaboration.Excellent oral and written communication.Ability to work independently, multitask and shift workload according to department/team priorities.Strong planning and organizational skills and experience managing and delivering on multiple priorities in a timely manner.Ability to demonstrate critical thinking while analyzing / resolving issues and improving processes.Proficiency in Microsoft Office (e.g., Word, Excel, PowerPoint) and PDF editor software (e.g., Adobe Professional, Foxit).High attention to detail. PREFERRED SKILLS: Experience processing documents within an EDMS (e.g., Veeva Vault Quality, Master Control).Ability to see the big picture regarding overall process.Ability to demonstrate critical thinking while analyzing / resolving issues and improving processesDemonstrated ability to follow-up on open action itemsExcellent verbal and written communication skills within a global environment.Ability to work independently, multitask and shift workload according to department/team priorities.   skills: Accounts Receivable, 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.
    • deerfield, illinois
    • contract
    • $40 - $45.28 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: Deerfield, Illinois job type: Contract salary: $40.00 - 45.28 per hour work hours: 9 to 5 education: Associate   responsibilities: Support global product UDI regulatory compliance throughout the product lifecycle:Responsible for aligning with internal requirements and accountable for managing accurate UDI medical device data entered in regulated UDI databases, enabling compliance with UDI regulations in all appropriate global markets (e.g., USA, China, Europe, South Korea, Saudi Arabia)Collaborate with data management professionals, UDI data owners, and sustaining engineering resources to capture, process, and maintain UDI data in internal and external systemsRepresent on internal teams, collaborating on process and system development, and testingEffectively communicate with all internal stakeholders (e.g., R&D, manufacturing etc.) to enable UDI compliant solution implementation and maintenanceEngage with Global Business Unit Regulatory teams and Regional Regulatory teams to ensure regulatory activities are in alignment with business requirements  qualifications: Required education: Minimum Two-Year Degree, prefer Bachelor's degree in Information technology (IT) or a related medical, science, engineering discipline Required experience: Minimum of 1 year of experience in data management Proficiency with Microsoft systems (Excel, PowerPoint, and Word)Attention to detailAbility to: Communicate effectively verbally and in writing (English)Communicate with diverse audiences and personnelManage small projects, including stakeholder, schedule, and priority managementContribute to technical documentsCollaborate within matrixed and/or cross-functional teamsWork with people from various disciplines and culturesActively participate and/or lead online meetingsThink analytically with good problem-solving skillsOrganize and track complex informationExercise good and ethical judgment within policy and regulationsRecognize compliance risks and escalate when appropriate Prefer those who have experience and/or knowledge, including configuration requirements and testing: SAP and/or JDE ERP systems and solutionsProduct and/or master data master solutions and systems (PDM, PIM, MDM)   skills: 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 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: Deerfield, Illinois job type: Contract salary: $40.00 - 45.28 per hour work hours: 9 to 5 education: Associate   responsibilities: Support global product UDI regulatory compliance throughout the product lifecycle:Responsible for aligning with internal requirements and accountable for managing accurate UDI medical device data entered in regulated UDI databases, enabling compliance with UDI regulations in all appropriate global markets (e.g., USA, China, Europe, South Korea, Saudi Arabia)Collaborate with data management professionals, UDI data owners, and sustaining engineering resources to capture, process, and maintain UDI data in internal and external systemsRepresent on internal teams, collaborating on process and system development, and testingEffectively communicate with all internal stakeholders (e.g., R&D, manufacturing etc.) to enable UDI compliant solution implementation and maintenanceEngage with Global Business Unit Regulatory teams and Regional Regulatory teams to ensure regulatory activities are in alignment with business requirements  qualifications: Required education: Minimum Two-Year Degree, prefer Bachelor's degree in Information technology (IT) or a related medical, science, engineering discipline Required experience: Minimum of 1 year of experience in data management Proficiency with Microsoft systems (Excel, PowerPoint, and Word)Attention to detailAbility to: Communicate effectively verbally and in writing (English)Communicate with diverse audiences and personnelManage small projects, including stakeholder, schedule, and priority managementContribute to technical documentsCollaborate within matrixed and/or cross-functional teamsWork with people from various disciplines and culturesActively participate and/or lead online meetingsThink analytically with good problem-solving skillsOrganize and track complex informationExercise good and ethical judgment within policy and regulationsRecognize compliance risks and escalate when appropriate Prefer those who have experience and/or knowledge, including configuration requirements and testing: SAP and/or JDE ERP systems and solutionsProduct and/or master data master solutions and systems (PDM, PIM, MDM)   skills: 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.
    • la grange, illinois
    • temp to perm
    • $24 - $26 per hour
    job summary: Analytical Lab Chemist II - EXCLUSIVE - $24-$26 - (depends on exp) 3rd shit - Shift - 11am-8am   location: La Grange, Illinois job type: Temporary salary: $24 - 26 per hour work hours: 11 to 7 education: Bachelors   responsibilities: Assist Laboratory Manager with training all laboratory personnel in Wet Chemistry.Communicate with Upper Management.Assist with reviewing and updating existing method procedures.Perform method verifications.Test incoming raw chemicals.Test in-process and batch samples, give routine batch adjustments.Witness of actives into batches.Issuing approval, rejection, hold and transfer tags.Test line start up samples and finished good line samples.Follow and observe batch transfer procedure.Test and receive incoming tankers.Maintain and calibrate test equipment per schedule.Operate and troubleshoot HPLC.Operate and troubleshoot GC.Notify Lab lead, supervisor or manager of any OOS results.Issuing approval, rejection, hold and transfer tags.Follow cGMPs.and GLP.Observe safety rules.Special projects as assigned.   qualifications: BS/BA Degree in Chemistry or equivalent. Minimum of 5-7 years experience in HBA, Cosmetic or Drug industry or equivalent. Knowledge of cGMPs. Operational Knowledge of: Gas Chromatograph, High Pressure Liquid Chromatograph, Infrared Spectroscopy, pH meter, viscometer, UV-Vis. Good Computer Skills. Good Communication Skills. Cooperative. Fluent in English (reading & speaking).   skills: Analytical Chemistry 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: Analytical Lab Chemist II - EXCLUSIVE - $24-$26 - (depends on exp) 3rd shit - Shift - 11am-8am   location: La Grange, Illinois job type: Temporary salary: $24 - 26 per hour work hours: 11 to 7 education: Bachelors   responsibilities: Assist Laboratory Manager with training all laboratory personnel in Wet Chemistry.Communicate with Upper Management.Assist with reviewing and updating existing method procedures.Perform method verifications.Test incoming raw chemicals.Test in-process and batch samples, give routine batch adjustments.Witness of actives into batches.Issuing approval, rejection, hold and transfer tags.Test line start up samples and finished good line samples.Follow and observe batch transfer procedure.Test and receive incoming tankers.Maintain and calibrate test equipment per schedule.Operate and troubleshoot HPLC.Operate and troubleshoot GC.Notify Lab lead, supervisor or manager of any OOS results.Issuing approval, rejection, hold and transfer tags.Follow cGMPs.and GLP.Observe safety rules.Special projects as assigned.   qualifications: BS/BA Degree in Chemistry or equivalent. Minimum of 5-7 years experience in HBA, Cosmetic or Drug industry or equivalent. Knowledge of cGMPs. Operational Knowledge of: Gas Chromatograph, High Pressure Liquid Chromatograph, Infrared Spectroscopy, pH meter, viscometer, UV-Vis. Good Computer Skills. Good Communication Skills. Cooperative. Fluent in English (reading & speaking).   skills: Analytical Chemistry 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.
    • la grange, illinois
    • temp to perm
    • $24 - $26 per hour
    job summary: Analytical Lab Chemist II $24-$26 - (depends on exp) 2 nd Shift - 3pm - 11am (M-F)   location: La Grange, Illinois job type: Temporary salary: $24 - 26 per hour work hours: 3 to 11 education: Bachelors   responsibilities: Assist Laboratory Manager with training all laboratory personnel in Wet Chemistry.Communicate with Upper Management.Assist with reviewing and updating existing method procedures.Perform method verifications.Test incoming raw chemicals.Test in-process and batch samples, give routine batch adjustments.Witness of actives into batches.Issuing approval, rejection, hold and transfer tags.Test line start up samples and finished good line samples.Follow and observe batch transfer procedure.Test and receive incoming tankers.Maintain and calibrate test equipment per schedule.Operate and troubleshoot HPLC.Operate and troubleshoot GC.Notify Lab lead, supervisor or manager of any OOS results.Issuing approval, rejection, hold and transfer tags.Follow cGMPs.and GLP.Observe safety rules.Special projects as assigned.  qualifications: Job Qualifications: BS/BA Degree in Chemistry or equivalent. Minimum of 5-7 years experience in HBA, Cosmetic or Drug industry or equivalent. Knowledge of cGMPs. Operational Knowledge of: Gas Chromatograph, High Pressure Liquid Chromatograph, Infrared Spectroscopy, pH meter, viscometer, UV-Vis. Good Computer Skills. Good Communication Skills. Cooperative. Fluent in English (reading & speaking).   skills: Analytical Chemistry 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: Analytical Lab Chemist II $24-$26 - (depends on exp) 2 nd Shift - 3pm - 11am (M-F)   location: La Grange, Illinois job type: Temporary salary: $24 - 26 per hour work hours: 3 to 11 education: Bachelors   responsibilities: Assist Laboratory Manager with training all laboratory personnel in Wet Chemistry.Communicate with Upper Management.Assist with reviewing and updating existing method procedures.Perform method verifications.Test incoming raw chemicals.Test in-process and batch samples, give routine batch adjustments.Witness of actives into batches.Issuing approval, rejection, hold and transfer tags.Test line start up samples and finished good line samples.Follow and observe batch transfer procedure.Test and receive incoming tankers.Maintain and calibrate test equipment per schedule.Operate and troubleshoot HPLC.Operate and troubleshoot GC.Notify Lab lead, supervisor or manager of any OOS results.Issuing approval, rejection, hold and transfer tags.Follow cGMPs.and GLP.Observe safety rules.Special projects as assigned.  qualifications: Job Qualifications: BS/BA Degree in Chemistry or equivalent. Minimum of 5-7 years experience in HBA, Cosmetic or Drug industry or equivalent. Knowledge of cGMPs. Operational Knowledge of: Gas Chromatograph, High Pressure Liquid Chromatograph, Infrared Spectroscopy, pH meter, viscometer, UV-Vis. Good Computer Skills. Good Communication Skills. Cooperative. Fluent in English (reading & speaking).   skills: Analytical Chemistry 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.
    • northbrook, illinois
    • contract
    • $33.44 - $39.34 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. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now! 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: Northbrook, Illinois job type: Contract salary: $33.44 - 39.34 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Supports the QA staff by offering consultation, advice, and subject matter expertise regarding QMS document control requirements.Processes and manages approximately 125 quality documents per month.Able to negotiate and build consensus for plans and priorities and able to develop effective relationships through collaboration.   qualifications: Bachelor of Arts/ Bachelor of Science degree BS/BA1-3 years working experience in the pharmaceutical industry, 1 of which should be within Quality Assurance and/or within SOP writing, Process Improvement, or similar discipline.Proficiency in Microsoft Office tools (e.g., Word, Excel, PowerPoint) and PDF editor software (e.g., Adobe Professional, Foxit).Experience processing documents for review and approval using an electronic system.Experience with working in a role that requires multitasking and completing tasks based on changing priorities. Potential of 15-30 families of documents working on at one time.Excels in Customer service, interacting with authors, and critical thinking skills.Advanced Microsoft Office skills; extensive experience with Word and using styles and formatting.Excellent oral and written communication.Strong planning and organizational skills and experience managing multiple priorities simultaneously.High attention to detail.Has the initiative and desire to learn new things, take on new work independently, and a desire for excellent customer service.Sharp, quick learner, polished, independent.Strong interpersonal skills and multi-cultural /intercultural awareness  skills: SOP, 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. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now! 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: Northbrook, Illinois job type: Contract salary: $33.44 - 39.34 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Supports the QA staff by offering consultation, advice, and subject matter expertise regarding QMS document control requirements.Processes and manages approximately 125 quality documents per month.Able to negotiate and build consensus for plans and priorities and able to develop effective relationships through collaboration.   qualifications: Bachelor of Arts/ Bachelor of Science degree BS/BA1-3 years working experience in the pharmaceutical industry, 1 of which should be within Quality Assurance and/or within SOP writing, Process Improvement, or similar discipline.Proficiency in Microsoft Office tools (e.g., Word, Excel, PowerPoint) and PDF editor software (e.g., Adobe Professional, Foxit).Experience processing documents for review and approval using an electronic system.Experience with working in a role that requires multitasking and completing tasks based on changing priorities. Potential of 15-30 families of documents working on at one time.Excels in Customer service, interacting with authors, and critical thinking skills.Advanced Microsoft Office skills; extensive experience with Word and using styles and formatting.Excellent oral and written communication.Strong planning and organizational skills and experience managing multiple priorities simultaneously.High attention to detail.Has the initiative and desire to learn new things, take on new work independently, and a desire for excellent customer service.Sharp, quick learner, polished, independent.Strong interpersonal skills and multi-cultural /intercultural awareness  skills: SOP, 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.
    • northbrook, illinois
    • contract
    • $39 - $45.90 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now! 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: Northbrook, Illinois job type: Contract salary: $39.00 - 45.90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Project manages and executes tasks associated with the Change Control quality system following management guidance and oversight. Maintains & monitors the applicable change control system, associated databases to ensure that records are in a compliant state and generates metrics for routine reporting. Assures company compliance with global regulations, corporate standards and SOPs for Change Control and general quality systems. Supports additional Quality Assurance initiatives as requested. Executes tasks associated with all company quality systems as directed, with a focus on change control, as an individual contributor and updates related databases and/or tracking tools in a timely manner. Generates status reports as required and maintains relevant change control databases and/or project management plans.Is a subject matter expert (SME) for the global change control system and interfaces with local affiliate QA functions to integrate local change control activity with governing corporate change control(s). Acts a resource for affiliate QA with respect to change control system.Project Management of complex multi-faceted strategic change controls as it relates to business objectives and assurance of change control implementation for all globally impacted stakeholders.Initiates, evaluates, assesses and tracks change controls utilizing effective project management skills and tools to monitor global action items / deliverables to target due dates. Ensures compliant and timely implementation of changes.Utilizes technical skills and quality assurance experience to identify areas of concern in both electronic and paper-based change control quality systems, as well as specific project deliverables. Evaluates and assesses risks to facilitate timely notification to management and provides proposals for resolution.Coordinates the collection and tabulation of metrics related to the change control quality system as directed by management. Monitors system for positive and adverse trends.Assures global company adherence and compliance with corporate policies, SOPs and global regulatory standards. Identifies issues and initiates corrective and/or preventive actions as required.Supports any additional quality activities related to the performance of gap assessments and/or resolution of any identified risks as requested.Effectively communicates with departmental and global cross-functional teams to support and facilitate change control project deliverables.Responsible for the storage and maintenance of quality-controlled documentation related to change control activity.Executes tasks associated with general quality systems, and more specifically, the company global change control quality system. Project manages any assigned change control related activity and deliverables to completion in partnership with global company quality assurance affiliates and external business partners as applicable. Assists, develops and manages timelines to maintain compliance to company project timelines, SOPs, standards and global regulatory requirements.This role reports to the QA Commercial Quality Representative of either Latin America or Russia as applicable. Works closely with other areas such as Regulatory Affairs, PV, Legal, Commercial, Supply Chain, Market Access, Global Project Management and Product and Project Management.  qualifications: Required Must be fluent in Spanish with strong technical writing and speaking skills in English.Strong TrackWise skills.Minimum BA/BS with minimum 5 years of industry experience with a minimum of 3 years QA / QC experience and 2 years of project management.Knowledge of global GMPs and other industry regulationsStrong, effective communication and interpersonal skills with an emphasis on cultural awareness.Ethical, results-oriented professional with attention to detail.Individual contributor with understanding and commitment to team success and efficiently executes assigned tasks per management direction.Confident & professional representation of the company to external stakeholders including international health care professionals.Requires strong project management skills and ability to execute change control responsibilities. Preferred: GMP manufacturing and/or Commercial affiliate experience  skills: Quality control, SOP, 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 find 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. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now! 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: Northbrook, Illinois job type: Contract salary: $39.00 - 45.90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Project manages and executes tasks associated with the Change Control quality system following management guidance and oversight. Maintains & monitors the applicable change control system, associated databases to ensure that records are in a compliant state and generates metrics for routine reporting. Assures company compliance with global regulations, corporate standards and SOPs for Change Control and general quality systems. Supports additional Quality Assurance initiatives as requested. Executes tasks associated with all company quality systems as directed, with a focus on change control, as an individual contributor and updates related databases and/or tracking tools in a timely manner. Generates status reports as required and maintains relevant change control databases and/or project management plans.Is a subject matter expert (SME) for the global change control system and interfaces with local affiliate QA functions to integrate local change control activity with governing corporate change control(s). Acts a resource for affiliate QA with respect to change control system.Project Management of complex multi-faceted strategic change controls as it relates to business objectives and assurance of change control implementation for all globally impacted stakeholders.Initiates, evaluates, assesses and tracks change controls utilizing effective project management skills and tools to monitor global action items / deliverables to target due dates. Ensures compliant and timely implementation of changes.Utilizes technical skills and quality assurance experience to identify areas of concern in both electronic and paper-based change control quality systems, as well as specific project deliverables. Evaluates and assesses risks to facilitate timely notification to management and provides proposals for resolution.Coordinates the collection and tabulation of metrics related to the change control quality system as directed by management. Monitors system for positive and adverse trends.Assures global company adherence and compliance with corporate policies, SOPs and global regulatory standards. Identifies issues and initiates corrective and/or preventive actions as required.Supports any additional quality activities related to the performance of gap assessments and/or resolution of any identified risks as requested.Effectively communicates with departmental and global cross-functional teams to support and facilitate change control project deliverables.Responsible for the storage and maintenance of quality-controlled documentation related to change control activity.Executes tasks associated with general quality systems, and more specifically, the company global change control quality system. Project manages any assigned change control related activity and deliverables to completion in partnership with global company quality assurance affiliates and external business partners as applicable. Assists, develops and manages timelines to maintain compliance to company project timelines, SOPs, standards and global regulatory requirements.This role reports to the QA Commercial Quality Representative of either Latin America or Russia as applicable. Works closely with other areas such as Regulatory Affairs, PV, Legal, Commercial, Supply Chain, Market Access, Global Project Management and Product and Project Management.  qualifications: Required Must be fluent in Spanish with strong technical writing and speaking skills in English.Strong TrackWise skills.Minimum BA/BS with minimum 5 years of industry experience with a minimum of 3 years QA / QC experience and 2 years of project management.Knowledge of global GMPs and other industry regulationsStrong, effective communication and interpersonal skills with an emphasis on cultural awareness.Ethical, results-oriented professional with attention to detail.Individual contributor with understanding and commitment to team success and efficiently executes assigned tasks per management direction.Confident & professional representation of the company to external stakeholders including international health care professionals.Requires strong project management skills and ability to execute change control responsibilities. Preferred: GMP manufacturing and/or Commercial affiliate experience  skills: Quality control, SOP, 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.
    • northbrook, illinois (remote)
    • permanent
    • $80,000 - $95,000 per year
    job summary: Seeking a detail oriented Sr. QC reviewer to join our FSP team. The primary role of the Sr. QC Reviewer is to perform scientific quality review of regulatory documents to ensure date integrity and compliance with applicable regulatory requirements. This is a full-time remote position that offers aid holidays, PTO, medical and dental benefits.   location: Northbrook, Illinois job type: Permanent salary: $80,000 - 95,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Perform quality reviews of global regulatory documents and submissions including: clinical study reports (CSR), CSR appendices, CSR amendments, synopses, patient narratives, statistical analysis plans, investigator brochures, protocols, amendments, Investigational Medicinal Product Dossiers (IMPDs) and Common Technical Documents (CTDs) for content and data accuracy with sourcesEnsure the all documents meet designated requirements for formatting, consistency, grammar, style guidelines and publishing guidelines.   qualifications: Bachelor's degree required, Prefer Nursing or Scientific DegreeMaster's Degree preferred in Medical/Scientific fieldUnderstanding of the pharmaceutical drug development processMust have Quality Control experience in the Medical Writing fieldWorking knowledge of ICH and CFR regulatory guidelinesHigh proficiency with Windows based applications and medical/scientific publication databases/resourcesAbility to manage multiple priorities and meet deadlinesExcellent organizational and time management skillsStrong oral and written communication skillsTeam player with excellent interpersonal skills   skills: GCP (Good Clinical 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: Seeking a detail oriented Sr. QC reviewer to join our FSP team. The primary role of the Sr. QC Reviewer is to perform scientific quality review of regulatory documents to ensure date integrity and compliance with applicable regulatory requirements. This is a full-time remote position that offers aid holidays, PTO, medical and dental benefits.   location: Northbrook, Illinois job type: Permanent salary: $80,000 - 95,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Perform quality reviews of global regulatory documents and submissions including: clinical study reports (CSR), CSR appendices, CSR amendments, synopses, patient narratives, statistical analysis plans, investigator brochures, protocols, amendments, Investigational Medicinal Product Dossiers (IMPDs) and Common Technical Documents (CTDs) for content and data accuracy with sourcesEnsure the all documents meet designated requirements for formatting, consistency, grammar, style guidelines and publishing guidelines.   qualifications: Bachelor's degree required, Prefer Nursing or Scientific DegreeMaster's Degree preferred in Medical/Scientific fieldUnderstanding of the pharmaceutical drug development processMust have Quality Control experience in the Medical Writing fieldWorking knowledge of ICH and CFR regulatory guidelinesHigh proficiency with Windows based applications and medical/scientific publication databases/resourcesAbility to manage multiple priorities and meet deadlinesExcellent organizational and time management skillsStrong oral and written communication skillsTeam player with excellent interpersonal skills   skills: GCP (Good Clinical 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.
    • northbrook, illinois (remote)
    • permanent
    • $150,000 - $165,000 per year
    job summary: Seeking an experienced senior level Medical Writer. The ideal candidate should have 3+ years of regulatory writing experience.   location: Northbrook, Illinois job type: Permanent salary: $150,000 - 165,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: May include but not limited to the following: Under minimal supervision, writes and edits clinical study reports, protocols, informed consent forms, and other clinical and regulatory documents including Investigator Brochures and annual reports.Assists with the preparation of briefing documents, INDs, and other major submissions (BLAs, MAAs) as needed.Leads the process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts.Provides QC support for clinical regulatory documents as needed (cross-checking data and verifying content from source documents).Reviews case report forms, statistical analysis plans, and data tables and listings for content and format.Participates in clinical project team meetings.Ensures the quality of clinical regulatory documents by maintaining and promoting familiarity with ICH, GCP, and other standards.  qualifications: ? Education: Requires an advanced degree in a scientific discipline or a bachelor's degree with equivalent work experience. Experience: 3+ years experience writing/editing clinical regulatory documents including clinical study reportsPharmaceutical industry experience and background in biologics a plus Special Skills: Excellent writing, editing, attention to detail and verbal communication skillsAbility to critically analyze and synthesize complex scientific information from a broad range of scientific disciplines and clinical therapeutic areasProficiency in Microsoft WordFamiliarity with CTD, ICH, GCP and other standardsAbility to manage/prioritize multiple projects from conception to completion, working in a fast-paced environment  skills: GCP (Good Clinical 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: Seeking an experienced senior level Medical Writer. The ideal candidate should have 3+ years of regulatory writing experience.   location: Northbrook, Illinois job type: Permanent salary: $150,000 - 165,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: May include but not limited to the following: Under minimal supervision, writes and edits clinical study reports, protocols, informed consent forms, and other clinical and regulatory documents including Investigator Brochures and annual reports.Assists with the preparation of briefing documents, INDs, and other major submissions (BLAs, MAAs) as needed.Leads the process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts.Provides QC support for clinical regulatory documents as needed (cross-checking data and verifying content from source documents).Reviews case report forms, statistical analysis plans, and data tables and listings for content and format.Participates in clinical project team meetings.Ensures the quality of clinical regulatory documents by maintaining and promoting familiarity with ICH, GCP, and other standards.  qualifications: ? Education: Requires an advanced degree in a scientific discipline or a bachelor's degree with equivalent work experience. Experience: 3+ years experience writing/editing clinical regulatory documents including clinical study reportsPharmaceutical industry experience and background in biologics a plus Special Skills: Excellent writing, editing, attention to detail and verbal communication skillsAbility to critically analyze and synthesize complex scientific information from a broad range of scientific disciplines and clinical therapeutic areasProficiency in Microsoft WordFamiliarity with CTD, ICH, GCP and other standardsAbility to manage/prioritize multiple projects from conception to completion, working in a fast-paced environment  skills: GCP (Good Clinical 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.
    • northbrook, illinois (remote)
    • permanent
    • $160,000 - $175,000 per year
    job summary: Seeking an experienced Document Manager to lead the Oncology regulatory writing team. The ideal candidate should have 5+ years of specific Oncology regulatory writing experience and 3+ years of management experience.   location: Northbrook, Illinois job type: Permanent salary: $160,000 - 175,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Acts as a lead for complex documents and is responsible for leading document related writing activities, and coordinating and managing the writing tasks within a multidiscipline document working group Coordinates, manages and facilitates the tasks necessary for document drafting, review, and completion, meeting internal and external customer needs, within a document working group Develops and executes an agreed upon and complete document work plan, with all needed written tasks and subtask that enables the working group to work efficiently and effectively As a document specialist, provides intellectual leadership and contributes document knowledge and expertise to the document working group. May perform editorial activities, including review of work by writer. May perform writing tasks within a document working group including drafting and revision of drafts addressing all comments in collaboration with responsible content authors and scientific document lead to ensure document quality in regard to correctness of structure, content, language, and/or style.  qualifications: Education: Requires an advanced degree in a scientific discipline or a bachelor's degree with equivalent work experience. MS or PhD in biological science preferred. Experience: 6 + years experience writing high-quality clinical regulatory documents including clinical study reports across multiple therapeutic areas, including at least 3 years of experience in Oncology. Experience writing CSRs for pivotal/registration studies or writing clinical sections of licensing submissions required Pharmaceutical industry experience required Background in biologics a plus Special Skills: Excellent writing, editing, verbal and interpersonal communication skills and a strong attention to details Experience writing and editing ICH-compliant clinical regulatory documents according to CTD structure Ability to critically analyze, synthesize, and communicate/present complex scientific information from a broad range of scientific disciplines and clinical therapeutic areas Ability to adapt and work through conflicts to create consensus Proficiency in Microsoft Office applications Familiarity with CTD, ICH, GCP and other standards Ability to manage/prioritize multiple projects from conception to completion, working in a fast-paced environment  skills: GCP (Good Clinical 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: Seeking an experienced Document Manager to lead the Oncology regulatory writing team. The ideal candidate should have 5+ years of specific Oncology regulatory writing experience and 3+ years of management experience.   location: Northbrook, Illinois job type: Permanent salary: $160,000 - 175,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Acts as a lead for complex documents and is responsible for leading document related writing activities, and coordinating and managing the writing tasks within a multidiscipline document working group Coordinates, manages and facilitates the tasks necessary for document drafting, review, and completion, meeting internal and external customer needs, within a document working group Develops and executes an agreed upon and complete document work plan, with all needed written tasks and subtask that enables the working group to work efficiently and effectively As a document specialist, provides intellectual leadership and contributes document knowledge and expertise to the document working group. May perform editorial activities, including review of work by writer. May perform writing tasks within a document working group including drafting and revision of drafts addressing all comments in collaboration with responsible content authors and scientific document lead to ensure document quality in regard to correctness of structure, content, language, and/or style.  qualifications: Education: Requires an advanced degree in a scientific discipline or a bachelor's degree with equivalent work experience. MS or PhD in biological science preferred. Experience: 6 + years experience writing high-quality clinical regulatory documents including clinical study reports across multiple therapeutic areas, including at least 3 years of experience in Oncology. Experience writing CSRs for pivotal/registration studies or writing clinical sections of licensing submissions required Pharmaceutical industry experience required Background in biologics a plus Special Skills: Excellent writing, editing, verbal and interpersonal communication skills and a strong attention to details Experience writing and editing ICH-compliant clinical regulatory documents according to CTD structure Ability to critically analyze, synthesize, and communicate/present complex scientific information from a broad range of scientific disciplines and clinical therapeutic areas Ability to adapt and work through conflicts to create consensus Proficiency in Microsoft Office applications Familiarity with CTD, ICH, GCP and other standards Ability to manage/prioritize multiple projects from conception to completion, working in a fast-paced environment  skills: GCP (Good Clinical 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.
    • mount prospect, illinois
    • permanent
    • $65,000 - $70,000 per year
    job summary: Summary/Objective Within the Microbiology department, this role is responsible for the coordination of lab staff in daily workflow organization and sample troubleshooting in addition to routine and non-routine sample analysis. Additionally, monitors lab operations such that quality and behavioral procedures are being followed, supporting management in general operational oversight.   location: Mount Prospect, Illinois job type: Permanent salary: $65,000 - 70,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Plan and adjust daily laboratory workflow to meet the needs of sample volumes, client needs, and available staff. - Review and authorize test results, ensuring accuracy and traceability/documentation of activities performed. - Relay operational updates to management, communicating any customer impacts to Customer Service as appropriate. - Maintain technical proficiency and perform routine and non-routine microbiology analyses as required, including result interpretation. - Troubleshoot operation of equipment, assisting in maintenance as required. - Document and respond to QC failures, nonconformities & deviations and client out of specification results. - Participate in investigating non-conformances and development of corrective actions, working to implement required corrective actions at the bench level. - Perform and document training activities for department staff on all laboratory duties performed including safety procedures, general bench skills, method specific proficiencies and associated data system tasks. - Supports quality of lab operations by ensuring employees are following documented procedures and the team works to reduce non-conformances. - Participate in review and revision of applicable Standard Operating Procedures and Work Instructions. - Identify and assist with implementation of process improvements within the Microbiology Department. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - Bachelor's degree, preferably in Microbiology, or Associates degree with equivalent work experience. - 2 years working in a commercial lab environment with various food samples and methodologies. - Ability to distinguish colors as required for Microbiology testing. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment.   skills: Microbiology 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: Summary/Objective Within the Microbiology department, this role is responsible for the coordination of lab staff in daily workflow organization and sample troubleshooting in addition to routine and non-routine sample analysis. Additionally, monitors lab operations such that quality and behavioral procedures are being followed, supporting management in general operational oversight.   location: Mount Prospect, Illinois job type: Permanent salary: $65,000 - 70,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Plan and adjust daily laboratory workflow to meet the needs of sample volumes, client needs, and available staff. - Review and authorize test results, ensuring accuracy and traceability/documentation of activities performed. - Relay operational updates to management, communicating any customer impacts to Customer Service as appropriate. - Maintain technical proficiency and perform routine and non-routine microbiology analyses as required, including result interpretation. - Troubleshoot operation of equipment, assisting in maintenance as required. - Document and respond to QC failures, nonconformities & deviations and client out of specification results. - Participate in investigating non-conformances and development of corrective actions, working to implement required corrective actions at the bench level. - Perform and document training activities for department staff on all laboratory duties performed including safety procedures, general bench skills, method specific proficiencies and associated data system tasks. - Supports quality of lab operations by ensuring employees are following documented procedures and the team works to reduce non-conformances. - Participate in review and revision of applicable Standard Operating Procedures and Work Instructions. - Identify and assist with implementation of process improvements within the Microbiology Department. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - Bachelor's degree, preferably in Microbiology, or Associates degree with equivalent work experience. - 2 years working in a commercial lab environment with various food samples and methodologies. - Ability to distinguish colors as required for Microbiology testing. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment.   skills: Microbiology 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.

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