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8 jobs found in raleigh, north carolina

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    • raleigh, north carolina
    • permanent
    • $40,000 - $45,000 per year
    job summary: The successful candidate will assist Business Development Team in all aspects of sales for Scientific Consulting, Accounting, and Grants Management services. The Sales Associate will train under experienced Business Development professionals and will gain experience in inside and outside sales; Salesforce; other sales activities.   location: Raleigh, North Carolina job type: Permanent salary: $40,000 - 45,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Maintain Salesforce CRM.Serve as contact for press inquiries and press releases alongside BD Manager.Participate in prospective client calls and meetings. Attend conferences as needed.Prepare follow-up emails and other correspondence for prospective clients.Develop and release company newsletters in support of Marketing Associate as needed.Coordinate closely with all departments to support their sales & marketing needs.Stays abreast of competitors and sales trends.Excellent sales service to ensure high levels of customer satisfaction.Follow and achieve department's sales goals on a monthly, quarterly and yearly basis  qualifications: Bachelor's degree in Sales, Marketing, or similar field. A science degree with a desire to enter a career in Sales/Marketing is also acceptable.Understanding of basic sales and marketing principles.Ability to create sales and marketing materials.Passion for helping companies and entrepreneurs advance their scientific discoveries.Ability to learn new tasks quickly and adapt accordingly.Ability to work independently and efficiently in a dynamic, growing entrepreneurial environment.Exceptional organization skills.Detail-oriented.Ability to meet deadlines.Strong communication skills, both written and verbal.Ability to work well independently and in teams.  skills: Sales Training 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: The successful candidate will assist Business Development Team in all aspects of sales for Scientific Consulting, Accounting, and Grants Management services. The Sales Associate will train under experienced Business Development professionals and will gain experience in inside and outside sales; Salesforce; other sales activities.   location: Raleigh, North Carolina job type: Permanent salary: $40,000 - 45,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Maintain Salesforce CRM.Serve as contact for press inquiries and press releases alongside BD Manager.Participate in prospective client calls and meetings. Attend conferences as needed.Prepare follow-up emails and other correspondence for prospective clients.Develop and release company newsletters in support of Marketing Associate as needed.Coordinate closely with all departments to support their sales & marketing needs.Stays abreast of competitors and sales trends.Excellent sales service to ensure high levels of customer satisfaction.Follow and achieve department's sales goals on a monthly, quarterly and yearly basis  qualifications: Bachelor's degree in Sales, Marketing, or similar field. A science degree with a desire to enter a career in Sales/Marketing is also acceptable.Understanding of basic sales and marketing principles.Ability to create sales and marketing materials.Passion for helping companies and entrepreneurs advance their scientific discoveries.Ability to learn new tasks quickly and adapt accordingly.Ability to work independently and efficiently in a dynamic, growing entrepreneurial environment.Exceptional organization skills.Detail-oriented.Ability to meet deadlines.Strong communication skills, both written and verbal.Ability to work well independently and in teams.  skills: Sales Training 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.
    • morrisville, north carolina
    • contract
    • $28 - $32.20 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. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! 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: Morrisville, North Carolina job type: Contract salary: $28.00 - 32.20 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Company's RTP site.The Raw Material Associate I's responsibilities include, but are not limited to release testing of raw materials using compendia (USP, Ph. Eur, and JP/JPE) and analytical methods, as well as validation/transfer of analytical methods, and technical support of QC investigations.Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, and completing all training/course requirements while maintaining 100% compliance on all assignments.  qualifications: This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.  skills: Quality control, Chemistry, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! 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: Morrisville, North Carolina job type: Contract salary: $28.00 - 32.20 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the Company's RTP site.The Raw Material Associate I's responsibilities include, but are not limited to release testing of raw materials using compendia (USP, Ph. Eur, and JP/JPE) and analytical methods, as well as validation/transfer of analytical methods, and technical support of QC investigations.Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, and completing all training/course requirements while maintaining 100% compliance on all assignments.  qualifications: This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers.The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skills.  skills: Quality control, Chemistry, 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.
    • research triangle park, north carolina (remote)
    • contract
    • $32.48 - $38.22 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. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! 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: Durham, North Carolina job type: Contract salary: $32.48 - 38.22 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Senior Quality Assurance Associate is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance. Activities include, but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. Review and approval of batch related documentation (cGMP procedures, Master Production Records, Solution Lot records, protocols and reports) to support product dispositionReview of executed Batch Records, procedures, forms, master production recordsReview and approval of InvestigationsExecutes activities including; intermediate technical writing, intermediate investigation support (root cause analysis/impact assessment), project representation (moderate complexity)Supports resolution of both technical and compliance issues/gaps of moderate complexity. Aides in implementation of Quality Systems/System Improvements with some guidance, moderate technical problem solving (tools or enterprise systems) within function and across multiple functional areasAssists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by the companyControl and release of equipment from maintenance, validation, change control and product changeoverSupports and/or assists in GxP quality systems-related training. Provides some mentorship and training within and across functions  qualifications: Quality and Compliance experience (CFR, ICH, ISO, etc.)Biologics experience (Cell Culture and Purification Manufacturing experience)Experience with Trackwise and/or ORACLE/SAP  skills: Quality Assurance, Protein Purification, Cell Cultures, ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to 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. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! 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: Durham, North Carolina job type: Contract salary: $32.48 - 38.22 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Senior Quality Assurance Associate is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance. Activities include, but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. Review and approval of batch related documentation (cGMP procedures, Master Production Records, Solution Lot records, protocols and reports) to support product dispositionReview of executed Batch Records, procedures, forms, master production recordsReview and approval of InvestigationsExecutes activities including; intermediate technical writing, intermediate investigation support (root cause analysis/impact assessment), project representation (moderate complexity)Supports resolution of both technical and compliance issues/gaps of moderate complexity. Aides in implementation of Quality Systems/System Improvements with some guidance, moderate technical problem solving (tools or enterprise systems) within function and across multiple functional areasAssists Quality Assurance Management in additional responsibilities related to the day-to-day implementation of the Quality Management Systems required to maintain cGMP compliance, and ensure the safety, efficacy and purity of the products manufactured by the companyControl and release of equipment from maintenance, validation, change control and product changeoverSupports and/or assists in GxP quality systems-related training. Provides some mentorship and training within and across functions  qualifications: Quality and Compliance experience (CFR, ICH, ISO, etc.)Biologics experience (Cell Culture and Purification Manufacturing experience)Experience with Trackwise and/or ORACLE/SAP  skills: Quality Assurance, Protein Purification, Cell Cultures, ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • durham, north carolina
    • contract
    • $22.10 - $26 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: Durham, North Carolina job type: Contract salary: $22.10 - 26.00 per hour work hours: 9 to 5 education: Associate   responsibilities: Summary: The main function of a lab technician is to perform routine medical laboratory tests for the diagnosis, treatment and prevention of disease. A typical lab technician may work under the supervision of a medical technologist. Job Responsibilities: Set up, adjust, maintain and clean medical laboratory equipment.Analyze the results of tests and experiments to ensure conformity to specifications, using special mechanical and electrical devices.Analyze, gather and record test data to issue reports that use charts, graphs and narratives.Obtain specimens, cultivating, isolating and identifying microorganisms for analysis.May examine cells stained with dye to locate abnormalities.Consult with a pathologist to determine a final diagnosis when abnormal cells are found.   qualifications: Skills: Verbal and written communication skills, attention to detail, and problem solving skills.Basic ability to work independently and manage ones time.Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.Basic ability to analyze data and accurately document and record results. Education/Experience: High school diploma or GED required.Associate's degree in medical technology or vocational training preferred.  skills: GLP (Good Laboratory 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 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: Durham, North Carolina job type: Contract salary: $22.10 - 26.00 per hour work hours: 9 to 5 education: Associate   responsibilities: Summary: The main function of a lab technician is to perform routine medical laboratory tests for the diagnosis, treatment and prevention of disease. A typical lab technician may work under the supervision of a medical technologist. Job Responsibilities: Set up, adjust, maintain and clean medical laboratory equipment.Analyze the results of tests and experiments to ensure conformity to specifications, using special mechanical and electrical devices.Analyze, gather and record test data to issue reports that use charts, graphs and narratives.Obtain specimens, cultivating, isolating and identifying microorganisms for analysis.May examine cells stained with dye to locate abnormalities.Consult with a pathologist to determine a final diagnosis when abnormal cells are found.   qualifications: Skills: Verbal and written communication skills, attention to detail, and problem solving skills.Basic ability to work independently and manage ones time.Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.Basic ability to analyze data and accurately document and record results. Education/Experience: High school diploma or GED required.Associate's degree in medical technology or vocational training preferred.  skills: GLP (Good Laboratory 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.
    • holly springs, north carolina
    • temp to perm
    • $45 - $48 per hour
    job summary: Primary responsibilities for this position include performing tasks associated with method validations and transfers. The analyst will be responsible for ensuring that validation samples are tested and reviewed according to quality requirements and results reported are valid, accurate, and documented per applicable regulatory and corporate requirements. Analyst may be required to perform or participate in tasks associated with method validation and transfers   location: Holly Springs, North Carolina job type: Temporary salary: $45 - 48 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Performs testing and associated tasks without errors per applicable SOPs and protocols.Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written.Develops and maintains SOPsDevelops expertise in assigned assays/techniquesAuthors deviation and invalid assay assessmentsMay be required to perform shift work as required to support the operations  qualifications: 3+ years of laboratory experience OR equivalentIntermediate knowledge of GMPs, safety regulations and data integrityIntermediate knowledge of analytical methods and related instrumentation.LIMS experience preferredExperience performing cell culture activitiesExperience performing Virus Titer assays, Residual Infectious Virus assays and other virology based testing methods.Experience performing PCR  skills: Chemistry, 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: Primary responsibilities for this position include performing tasks associated with method validations and transfers. The analyst will be responsible for ensuring that validation samples are tested and reviewed according to quality requirements and results reported are valid, accurate, and documented per applicable regulatory and corporate requirements. Analyst may be required to perform or participate in tasks associated with method validation and transfers   location: Holly Springs, North Carolina job type: Temporary salary: $45 - 48 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Performs testing and associated tasks without errors per applicable SOPs and protocols.Complies with policies and procedures in order to maintain compliance with legal regulations, health and safety, and regulatory requirements as written.Develops and maintains SOPsDevelops expertise in assigned assays/techniquesAuthors deviation and invalid assay assessmentsMay be required to perform shift work as required to support the operations  qualifications: 3+ years of laboratory experience OR equivalentIntermediate knowledge of GMPs, safety regulations and data integrityIntermediate knowledge of analytical methods and related instrumentation.LIMS experience preferredExperience performing cell culture activitiesExperience performing Virus Titer assays, Residual Infectious Virus assays and other virology based testing methods.Experience performing PCR  skills: Chemistry, 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.
    • durham, north carolina
    • temporary
    • $36 - $38 per hour
    Are you seeking a job that involves technical writing and investigative skills in a manufacturing environment? In this 12-month contract position, you will lead investigations for minor Quality deviations and incidents, focus on improvement and risk reduction, identify root causes and make recommendations to correct. Contribute to metrics related to investigation process and CAPA effectiveness.  If you have a 4-year degree, possess technical knowledge of manufacturing processes,investigating and writing, apply today!salary: $36 - $38 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities• Responsibilities include the following: • Limited technical knowledge of Manufacturing equipment and processes – must demonstrate minor level of technical depth and process knowledge of Manufacturing operations • Authors and/or issues manufacturing documentation, including Batch Production Records, Solution Lot Records, Procedures, and Work Instructions to meet production schedule with high degree of supervision from key stakeholders and Management • Will support Manufacturing focused Change Controls, Corrective and Preventive Actions (CAPAs), and Planned Exceptions • Project Management and Project Execution – may participate in some small project(s) (minor in nature) and execute job tasks associated with the project • Partners with Manufacturing, Manufacturing Sciences, Engineering, Automation, Quality, Planning, and Materials Management to identify continuous improvement opportunitiesThe essential functions of this role include:working in a smoke free environmentwearing steel toe shoesSkillsInvestigationsManufacturingWriting - DocumentationQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Are you seeking a job that involves technical writing and investigative skills in a manufacturing environment? In this 12-month contract position, you will lead investigations for minor Quality deviations and incidents, focus on improvement and risk reduction, identify root causes and make recommendations to correct. Contribute to metrics related to investigation process and CAPA effectiveness.  If you have a 4-year degree, possess technical knowledge of manufacturing processes,investigating and writing, apply today!salary: $36 - $38 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities• Responsibilities include the following: • Limited technical knowledge of Manufacturing equipment and processes – must demonstrate minor level of technical depth and process knowledge of Manufacturing operations • Authors and/or issues manufacturing documentation, including Batch Production Records, Solution Lot Records, Procedures, and Work Instructions to meet production schedule with high degree of supervision from key stakeholders and Management • Will support Manufacturing focused Change Controls, Corrective and Preventive Actions (CAPAs), and Planned Exceptions • Project Management and Project Execution – may participate in some small project(s) (minor in nature) and execute job tasks associated with the project • Partners with Manufacturing, Manufacturing Sciences, Engineering, Automation, Quality, Planning, and Materials Management to identify continuous improvement opportunitiesThe essential functions of this role include:working in a smoke free environmentwearing steel toe shoesSkillsInvestigationsManufacturingWriting - DocumentationQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • durham, north carolina
    • contract
    • $23.84 - $28.05 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: Durham, North Carolina job type: Contract salary: $23.84 - 28.05 per hour work hours: 9 to 5 education: Associate   responsibilities: Under the supervision of the Microbiology Lab Supervisor, technician performs sample collection, microbiological and tissue culture tasks associated with new or modified products or processes, contamination control and sterilization operations. Supports the Quality Assurance Department by taking an active role in team sharing, problem solving tasks, team activities and team and plant-wide subgroups focusing on the plant goals of safety, quality, schedule and cost. Performs environmental monitoring (EM) for production areas, processes and personnel for evaluating microbial and particulate contamination using air samplers, settle plates, contact plates, and particle counters.Collects and tests product samples according to documented procedures.Maintains cell line cultures and microbial cultures.Duties may include cell harvesting, scheduling cell line maintenance, conducting routine media changes, reviving newly purchased cell, quantifying cell inoculum.Performs general laboratory tasks such as media preparation, autoclaving supplies, wash and prepare glassware, discard waste and cultures following appropriate practices.Performs / tracks routine preventive maintenance and monitoring of laboratory equipment and supplies.Maintains accurate and current records of all results and procedures.Must be able to ensure a high degree of accuracy in all tests results obtained.Complies with safety standards and Good Laboratory Practice standards.Interacts with production personnel to ensure product sample collection.  qualifications: Must have a minimum of a two-year Associate Degree with course work in chemistry and biology.Must Have (1) year experience in a microbiology laboratory technician or microbiology testing lab position.Requires good written and oral communication skills. Must be highly motivated, detail oriented, possess excellent organizational and problem-solving skills, and be effective as a team player.Must possess the ability to work independently and manage multiple priorities and multi-task projects.Must be an independent thinker, self-starter, and perform responsibilities under very limited supervision.Must have a working knowledge of spreadsheet applications and word processing to perform necessary tasks for preparing required correspondence, reports and communication.Must be flexible and be willing to work overtime as required.Prior experience with a high-performance work team system preferred.  skills: GLP (Good Laboratory Practice), Microbiology, Cell Cultures 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: Durham, North Carolina job type: Contract salary: $23.84 - 28.05 per hour work hours: 9 to 5 education: Associate   responsibilities: Under the supervision of the Microbiology Lab Supervisor, technician performs sample collection, microbiological and tissue culture tasks associated with new or modified products or processes, contamination control and sterilization operations. Supports the Quality Assurance Department by taking an active role in team sharing, problem solving tasks, team activities and team and plant-wide subgroups focusing on the plant goals of safety, quality, schedule and cost. Performs environmental monitoring (EM) for production areas, processes and personnel for evaluating microbial and particulate contamination using air samplers, settle plates, contact plates, and particle counters.Collects and tests product samples according to documented procedures.Maintains cell line cultures and microbial cultures.Duties may include cell harvesting, scheduling cell line maintenance, conducting routine media changes, reviving newly purchased cell, quantifying cell inoculum.Performs general laboratory tasks such as media preparation, autoclaving supplies, wash and prepare glassware, discard waste and cultures following appropriate practices.Performs / tracks routine preventive maintenance and monitoring of laboratory equipment and supplies.Maintains accurate and current records of all results and procedures.Must be able to ensure a high degree of accuracy in all tests results obtained.Complies with safety standards and Good Laboratory Practice standards.Interacts with production personnel to ensure product sample collection.  qualifications: Must have a minimum of a two-year Associate Degree with course work in chemistry and biology.Must Have (1) year experience in a microbiology laboratory technician or microbiology testing lab position.Requires good written and oral communication skills. Must be highly motivated, detail oriented, possess excellent organizational and problem-solving skills, and be effective as a team player.Must possess the ability to work independently and manage multiple priorities and multi-task projects.Must be an independent thinker, self-starter, and perform responsibilities under very limited supervision.Must have a working knowledge of spreadsheet applications and word processing to perform necessary tasks for preparing required correspondence, reports and communication.Must be flexible and be willing to work overtime as required.Prior experience with a high-performance work team system preferred.  skills: GLP (Good Laboratory Practice), Microbiology, Cell Cultures 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.
    • research triangle park, north carolina
    • contract
    • $27.37 - $32.20 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: Durham, North Carolina job type: Contract salary: $27.37 - 32.20 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the company's Drug Product site. This includes performing incoming sampling and inspections for various raw materials. The Raw Material Associate I's responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, container closures, and packaging components, while maintaining, robust and compliant cGMP documentation practices. Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments. This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers. The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.   qualifications: The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skillsMust be able to move 50 lbs with assistance of equipment.  skills: Quality control, 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 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: Durham, North Carolina job type: Contract salary: $27.37 - 32.20 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Quality Control Raw Materials Associate I is responsible for contributing to key functional, tactical, strategic and operational aspects of the Quality Control Raw Materials group at the company's Drug Product site. This includes performing incoming sampling and inspections for various raw materials. The Raw Material Associate I's responsibilities include, but are not limited to, training, sampling/inspection support for raw materials, including active pharmaceutical ingredients, container closures, and packaging components, while maintaining, robust and compliant cGMP documentation practices. Additional responsibilities include entering data into electronic laboratory information management system and inventory control systems, maintaining retention (retain) samples, and completing all training/course requirements while maintaining 100% compliance on all assignments. This position interfaces with QC Chemistry, Quality, Planning, Warehouse, and Manufacturing customers. The Associate I may also support the Supervisor/Manager for activities related to compliance with GMP, and identifying corrective actions on the floor.   qualifications: The Associate I should be able to work effectively both independently and within a team framework, requiring both robust written and verbal communication skillsMust be able to move 50 lbs with assistance of equipment.  skills: Quality control, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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