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3 jobs found in madison, wisconsin

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    • madison, wisconsin
    • permanent
    • $190,000 - $220,000 per year
    job summary: Job Description: The Principal Scientist, Product Support role will lead a variety of technical and scientific activities within Operations. This position will investigate issues through trending, troubleshooting, and root cause analysis, working closely with R&D, Quality, and Operations to design, develop, and implement corrective actions through use of the Quality Management System. This role will also serve as a subject matter expert leading Operations teams in analytical test method development, applied chemistry/biochemistry support, new product introduction, and continuous improvement efforts.   location: Madison, Wisconsin job type: Permanent salary: $190,000 - 220,000 per year work hours: 8 to 4 education: Masters   responsibilities: Essential Duties and Responsibilities Provide technical and product support leadership in Operations working cross-functionally with the Manufacturing Sciences, Production, QC, Supply Chain, R&D, and Quality teams.Lead troubleshooting of Out Of Specifications (OOS), non-conformances (NCMRs), product and process failure mode and effects analyses (FMEAs), and corrective action preventive action (CAPA) plans through root cause investigation, experiment design, study execution, data analysis, and reporting.Exercise subject matter expertise across diverse technical disciplines to guide key decisions within operations and on cross-functional teams.Clearly and accurately generate experimental protocols, draft work instruction procedures, characterize and develop test methods and test method improvements, summarizing activities through technical or investigative reports.Lead Operations teams for qualifying new raw materials and alternative supply channels for products.Provide thought leadership and mentorship.Analyze, track, and trend historical Production and Quality Control data.Program, operate, and troubleshoot complex instrumentation such as micro plate readers, high performance liquid chromatography (HPLC) systems, mass spectrometry (LCMS), Real-Time PCR instruments, and liquid handling automation.Oversee design and execution of complex studies, measurement systems analyses (MSAs) and designed experiments.Conduct bench level experiments within several product or technology areas to identify problems and discrepancies.Support and comply with the company's Quality Management System policies and procedures.Perform other related duties and special projects as assigned by management.Communicate to all levels within the company and thrives in a fast-paced, everchanging environment.Evidence of strong analytical, problem-solving skills and negotiating skills. Ability to make decisions with limited information and operate with autonomy.Strong documentation, attention-to-detail and procedure writing skills suitable for a GMP environment.Excellent oral and written communication, strong interpersonal skills.Demonstrated ability to develop/transfer and thoroughly document new processes and production procedures.Ability to interpret technical data and present findings to management.Ability to work in a fast paced ever changing environment.Strong leadership capability and excellent attention to detail to reduce errors.Ability to organize, present, and convey complex problems or issues within and across other functions.Ability to effectively work on many complex and varied projects at one time, with frequent changing priorities.Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.Support and comply with the company's Quality Management System policies and procedures.Regular and reliable attendance.Ability to work designated schedule.Ability to work nights and/or weekends.Ability to lift up to 50 pounds for approximately 5% of a typical working day.Ability to utilize lab equipment for 25% of a typical working day.Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.Ability to work on a computer and phone simultaneously.Ability to use a telephone through a headset.Ability to comply with any applicable personal protective equipment requirements.Ability and means to travel between Madison locations.Ability to travel 10% of working time away from work location, may include overnight/weekend travel. #LI-KH1 Qualifications Minimum Qualifications Bachelor's degree in Chemistry, Molecular Biology, or Life Sciences related field.16+ years of industry experience with biochemical and molecular based products.Proficient in Microsoft Office.Advanced knowledge in statistical and mathematical methods in biology/genetics, including experience with JMP software.Proficient in knowledge of IVD product Manufacturing processes, Product Design, and Development.Professional working knowledge with 21 CFR Part 820, ISO 13485, and/or cGMP structured environments.Authorization to work in the United States without sponsorship.Demonstrated ability to perform the Essential Duties of the position with or without accommodation.  qualifications: Preferred Qualifications Master's or Ph.D. degree in Chemistry, Molecular Biology, or Life Sciences related field.10+ years of experience with Medical Device Products in a Quality Control, Product Development or Product Support role.Experience working within Enterprise Resource Planning (ERP) systems such as SAP.Strong knowledge in Design for Six Sigma.Strong knowledge in basic and advanced continuous improvement methodologies/ principles such as LEAN Six Sigma and/or Practical Process Improvements (PPI).Experience with Project Management principles and practice.   skills: Molecular Biology, 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. 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: Job Description: The Principal Scientist, Product Support role will lead a variety of technical and scientific activities within Operations. This position will investigate issues through trending, troubleshooting, and root cause analysis, working closely with R&D, Quality, and Operations to design, develop, and implement corrective actions through use of the Quality Management System. This role will also serve as a subject matter expert leading Operations teams in analytical test method development, applied chemistry/biochemistry support, new product introduction, and continuous improvement efforts.   location: Madison, Wisconsin job type: Permanent salary: $190,000 - 220,000 per year work hours: 8 to 4 education: Masters   responsibilities: Essential Duties and Responsibilities Provide technical and product support leadership in Operations working cross-functionally with the Manufacturing Sciences, Production, QC, Supply Chain, R&D, and Quality teams.Lead troubleshooting of Out Of Specifications (OOS), non-conformances (NCMRs), product and process failure mode and effects analyses (FMEAs), and corrective action preventive action (CAPA) plans through root cause investigation, experiment design, study execution, data analysis, and reporting.Exercise subject matter expertise across diverse technical disciplines to guide key decisions within operations and on cross-functional teams.Clearly and accurately generate experimental protocols, draft work instruction procedures, characterize and develop test methods and test method improvements, summarizing activities through technical or investigative reports.Lead Operations teams for qualifying new raw materials and alternative supply channels for products.Provide thought leadership and mentorship.Analyze, track, and trend historical Production and Quality Control data.Program, operate, and troubleshoot complex instrumentation such as micro plate readers, high performance liquid chromatography (HPLC) systems, mass spectrometry (LCMS), Real-Time PCR instruments, and liquid handling automation.Oversee design and execution of complex studies, measurement systems analyses (MSAs) and designed experiments.Conduct bench level experiments within several product or technology areas to identify problems and discrepancies.Support and comply with the company's Quality Management System policies and procedures.Perform other related duties and special projects as assigned by management.Communicate to all levels within the company and thrives in a fast-paced, everchanging environment.Evidence of strong analytical, problem-solving skills and negotiating skills. Ability to make decisions with limited information and operate with autonomy.Strong documentation, attention-to-detail and procedure writing skills suitable for a GMP environment.Excellent oral and written communication, strong interpersonal skills.Demonstrated ability to develop/transfer and thoroughly document new processes and production procedures.Ability to interpret technical data and present findings to management.Ability to work in a fast paced ever changing environment.Strong leadership capability and excellent attention to detail to reduce errors.Ability to organize, present, and convey complex problems or issues within and across other functions.Ability to effectively work on many complex and varied projects at one time, with frequent changing priorities.Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork.Support and comply with the company's Quality Management System policies and procedures.Regular and reliable attendance.Ability to work designated schedule.Ability to work nights and/or weekends.Ability to lift up to 50 pounds for approximately 5% of a typical working day.Ability to utilize lab equipment for 25% of a typical working day.Ability to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.Ability to grasp with both hands; pinch with thumb and forefinger; turn with hand/arm; reach above shoulder height.Ability to work on a computer and phone simultaneously.Ability to use a telephone through a headset.Ability to comply with any applicable personal protective equipment requirements.Ability and means to travel between Madison locations.Ability to travel 10% of working time away from work location, may include overnight/weekend travel. #LI-KH1 Qualifications Minimum Qualifications Bachelor's degree in Chemistry, Molecular Biology, or Life Sciences related field.16+ years of industry experience with biochemical and molecular based products.Proficient in Microsoft Office.Advanced knowledge in statistical and mathematical methods in biology/genetics, including experience with JMP software.Proficient in knowledge of IVD product Manufacturing processes, Product Design, and Development.Professional working knowledge with 21 CFR Part 820, ISO 13485, and/or cGMP structured environments.Authorization to work in the United States without sponsorship.Demonstrated ability to perform the Essential Duties of the position with or without accommodation.  qualifications: Preferred Qualifications Master's or Ph.D. degree in Chemistry, Molecular Biology, or Life Sciences related field.10+ years of experience with Medical Device Products in a Quality Control, Product Development or Product Support role.Experience working within Enterprise Resource Planning (ERP) systems such as SAP.Strong knowledge in Design for Six Sigma.Strong knowledge in basic and advanced continuous improvement methodologies/ principles such as LEAN Six Sigma and/or Practical Process Improvements (PPI).Experience with Project Management principles and practice.   skills: Molecular Biology, 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. 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.
    • verona, wisconsin
    • permanent
    • $41,600 - $52,000 per year
    job summary: Randstad is the #1 HR Services Company in the World and we are sourcing for a QC Chemist position in the Madison, WI area. The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $41,600 - 52,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Quality control, HPLC, SOP, Quality Assurance, Biology, Chemistry, 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. 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 QC Chemist position in the Madison, WI area. The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $41,600 - 52,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Quality control, HPLC, SOP, Quality Assurance, Biology, Chemistry, 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. 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.
    • madison, wisconsin
    • permanent
    • $97,000 - $97,500 per year
    job summary: OUR TEAM: We are a motivated and caring team of individuals that support one another in providing quality assurance to existing products and new product development. We do this by partnering with our colleagues throughout the Promega organization, including Manufacturing, Quality Control, Research and Development, Marketing, Quality Systems, Technical Services, and others. JOB OBJECTIVE: Through their specified review, approval, and planning roles, QA Scientists apply their technical and quality system knowledge to assure internal and external customers that:   location: Madison, Wisconsin job type: Permanent salary: $97,000 - 97,500 per year work hours: 9 to 5 education: Bachelors   responsibilities: 1. Promega catalog and custom products meet their predetermined performance, process, and system requirements for quality. 2. Product and Process Changes and Quarantine disposition plans are implemented according to established procedures. 3. Technical literature (PPIs, labels, Technical Bulletins etc) are accurate and consistent. 4. Product performance claims and release criteria are based on objective data analysis. CORE DUTIES: Note that the emphasis placed on the essential duties listed here will vary by individual, depending on the focus and balance of that person's specific responsibilities. 1. Audit, data review, and approve product batch records for the next manufacturing step or availability in inventory. 2. Review and approve Manufacturing and Quality Control Protocols for catalog and custom products. 3. Review and approve product labels. 4. Establish and approve shelf-life assignments for catalog and custom products in cooperation with Manufacturing, Marketing, Regulatory Affairs and R&D staff. This includes approval of study design, data review, and change approval. 5. Review and approval of Technical Bulletins and Technical Manuals (performance and application claim accuracy and validity), including final release for publication. 6. Review and approve Promega Product Information (PPI) specification sheets and Certificates of Analysis; initiation, completion and issuance of these documents as required for custom products and some catalog products. 7. Assess the scope and inventory impact of nonconforming product situations; approving disposition plans of inventory product under quarantine; assisting in the disposition planning for nonconforming product in branch inventories. 8. Assist in the preparation, review and approval of design control documents. 9. Initiate, implement, review and/or approve Product and Process Change Plans. 10. Review, implement, and/or participate in Corrective and Preventive Action plans. 11. Review, implement, and participate in product and process validation planning. 12. Review, implement, and participate in complaint investigation planning. 13. Participate in process mapping and SOP development as directed. 14. Write SOPs as assigned. 15. Participate in team meetings to resolve planning and technical issues. Propose constructive solutions to existing problems. 16. Evaluate risks based on customer, technical, business and regulatory factors, provide options and recommendations to mitigate risk. 17. Consider basic regulatory requirements in product or process issues. 18. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others. 19. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 20. Understand and comply with ethical, legal and regulatory requirements applicable to our business. OCCASIONAL DUTIES: 1. Organize, facilitate, or lead meetings to discuss review findings and planning issues. 2. Represent Promega in support of technical sales at national and international trade shows and exhibitions, or attend relevant scientific meetings as requested. 3. Contact customers directly about quality issues or questions as directed. 4. Organize and implement training programs in areas of expertise and experience. 5. Participate in continuous improvement projects.   qualifications: KEY QUALIFICATIONS: 1. B.S. degree with a minimum of 7 years work experience in a relevant industry with quality control, quality assurance, or manufacturing responsibilities. 2. Working knowledge and direct application experience of the requirements of quality assurance systems in a manufacturing and/or product development or process development environment. 3. Proficiency with basic word processing and spreadsheet software programs. 4. Ability to apply basic statistical concepts to analytical data, process validation, and Quality Assurance activities. 5. A demonstrable track record of process improvement and effective procedure writing and revision. 6. Able to develop concise, clear and accurate written communication. 7. Proven ability to work constructively with a broad range of people. PREFERRED QUALIFICATIONS: 1. In-depth technical knowledge in genomics, protein analysis, or cellular analysis evidenced by peer-reviewed publications. 2. Work experience in Quality Assurance from a regulated industry. PHYSICAL DEMANDS: 1. Visual acuity required for physical inspection of finished product and raw materials and accompanying documentation. 2. Ability to wear basic safety apparel (safety glasses or goggles, lab coats, protective gloves). 3. Ability to use computers in an interactive manner for extended periods of time.   skills: Biology, 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: OUR TEAM: We are a motivated and caring team of individuals that support one another in providing quality assurance to existing products and new product development. We do this by partnering with our colleagues throughout the Promega organization, including Manufacturing, Quality Control, Research and Development, Marketing, Quality Systems, Technical Services, and others. JOB OBJECTIVE: Through their specified review, approval, and planning roles, QA Scientists apply their technical and quality system knowledge to assure internal and external customers that:   location: Madison, Wisconsin job type: Permanent salary: $97,000 - 97,500 per year work hours: 9 to 5 education: Bachelors   responsibilities: 1. Promega catalog and custom products meet their predetermined performance, process, and system requirements for quality. 2. Product and Process Changes and Quarantine disposition plans are implemented according to established procedures. 3. Technical literature (PPIs, labels, Technical Bulletins etc) are accurate and consistent. 4. Product performance claims and release criteria are based on objective data analysis. CORE DUTIES: Note that the emphasis placed on the essential duties listed here will vary by individual, depending on the focus and balance of that person's specific responsibilities. 1. Audit, data review, and approve product batch records for the next manufacturing step or availability in inventory. 2. Review and approve Manufacturing and Quality Control Protocols for catalog and custom products. 3. Review and approve product labels. 4. Establish and approve shelf-life assignments for catalog and custom products in cooperation with Manufacturing, Marketing, Regulatory Affairs and R&D staff. This includes approval of study design, data review, and change approval. 5. Review and approval of Technical Bulletins and Technical Manuals (performance and application claim accuracy and validity), including final release for publication. 6. Review and approve Promega Product Information (PPI) specification sheets and Certificates of Analysis; initiation, completion and issuance of these documents as required for custom products and some catalog products. 7. Assess the scope and inventory impact of nonconforming product situations; approving disposition plans of inventory product under quarantine; assisting in the disposition planning for nonconforming product in branch inventories. 8. Assist in the preparation, review and approval of design control documents. 9. Initiate, implement, review and/or approve Product and Process Change Plans. 10. Review, implement, and/or participate in Corrective and Preventive Action plans. 11. Review, implement, and participate in product and process validation planning. 12. Review, implement, and participate in complaint investigation planning. 13. Participate in process mapping and SOP development as directed. 14. Write SOPs as assigned. 15. Participate in team meetings to resolve planning and technical issues. Propose constructive solutions to existing problems. 16. Evaluate risks based on customer, technical, business and regulatory factors, provide options and recommendations to mitigate risk. 17. Consider basic regulatory requirements in product or process issues. 18. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others. 19. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 20. Understand and comply with ethical, legal and regulatory requirements applicable to our business. OCCASIONAL DUTIES: 1. Organize, facilitate, or lead meetings to discuss review findings and planning issues. 2. Represent Promega in support of technical sales at national and international trade shows and exhibitions, or attend relevant scientific meetings as requested. 3. Contact customers directly about quality issues or questions as directed. 4. Organize and implement training programs in areas of expertise and experience. 5. Participate in continuous improvement projects.   qualifications: KEY QUALIFICATIONS: 1. B.S. degree with a minimum of 7 years work experience in a relevant industry with quality control, quality assurance, or manufacturing responsibilities. 2. Working knowledge and direct application experience of the requirements of quality assurance systems in a manufacturing and/or product development or process development environment. 3. Proficiency with basic word processing and spreadsheet software programs. 4. Ability to apply basic statistical concepts to analytical data, process validation, and Quality Assurance activities. 5. A demonstrable track record of process improvement and effective procedure writing and revision. 6. Able to develop concise, clear and accurate written communication. 7. Proven ability to work constructively with a broad range of people. PREFERRED QUALIFICATIONS: 1. In-depth technical knowledge in genomics, protein analysis, or cellular analysis evidenced by peer-reviewed publications. 2. Work experience in Quality Assurance from a regulated industry. PHYSICAL DEMANDS: 1. Visual acuity required for physical inspection of finished product and raw materials and accompanying documentation. 2. Ability to wear basic safety apparel (safety glasses or goggles, lab coats, protective gloves). 3. Ability to use computers in an interactive manner for extended periods of time.   skills: Biology, 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.

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