Quality Control Scientist

job summary: The QC Scientist I•Raw Materials will be accountable for executing and troubleshooting a variety of laboratory test methods, defining the requirements for implementation of procedures, processes and assays within QC, and identifying and implementing continuous improvement initiatives related to overall laboratory functionality.

location:

Westborough, Massachusetts job type: Contract salary: $50.00•57.65 per hour work hours: 9 to 5 education: Bachelors responsibilities: Execute and troubleshoot raw material testing in support of production activitiesPerform routine release sampling and managing testing of raw materials, such as compendial analysis per USP, Ph.

Eur., and JP monographs and general chapters, based on cGMP and internal proceduresDesign and perform testing in support of method transfer/validation/qualification/verificationReview/authorize data and perform analysis and interpretation of test results and trendsDesign and/or participate in method development; equipment qualification/validation studies; deviation and OOS investigationsPerform QC lab support activities including but not limited to sample management, reagent preparation, instrumentation maintenance, and instrument calibrationSupport and mentor junior team membersCollaborate with other network sites to share best practicesOther duties as required qualifications:

Required:

B.S. degree in chemistry, biological sciences or related field with 6+ years or M.S. degree with 4+ years of relevant experience in a GMP Quality Control rolePrior laboratory hands-on experience with a variety of techniques such as FTIR, Raman, Near-IR, HPLC analysis and other compendial assaysTechnical knowledge and experience in relevant areas of 21CFR, ICH, USP, Ph. Eur. and FDA guidance documents as well as cGXPs in support of clinical and commercial manufacturingProven knowledge in cGMP raw material program (RM sampling plans and testing requirements)Ensures inspection, testing and release timelines are met.

Strong understanding of data integrity requirements and regulatory requirements pertaining to biotechnology and pharmaceutical industries and proven experience analyzing experimental dataExperience using LIMS as an end user; Excellent technical writing and verbal communication skillsMust be capable of observing and adhering to lab safety standards and proceduresSuccessfully performs work independently with minimal instructionsStrong interpersonal skills, highly collaborative within a multi-discipline team and contributes to a supportive and positive work environment, strong knowledge of GMP, SOPs and quality control processes, and strong knowledge of quality systems and regulatory requirementsExcels in a fast-paced team environment, handles multiple tasks concurrently, and in a timely fashionHighly self-motivated and goal orientedWill support and demonstrate quality standards to ensure data of highest quality and works closely with team and other functional key stakeholders on the Astellas Operations team to execute work and will be expected to perform other duties and/or special projects as assigned

Preferred:

Experience in a Biotech/Pharmaceutical company with a high growth, fast-paced environmentExperience in qualification of analytical equipment, including those with computerized systemsExperience in method validation/qualification/verification/transfer

Working Conditions:

This role frequently requires long periods of sitting, standing and use of hands and regular motion to include bending, stooping, and lifting up to 20lbs.

This is an on-site role working in a cGMP regulated manufacturing facility. #LI-AM1 skills: SOP, Laboratory Information Management Systems (LIMS), Flow Cytometry, GMP (Good Manufacturing Practice), High Pressure Liquid Chromatography (HPLC),

Raw Materials 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. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. job detailssummary$50•$57.65 per hourcontractbachelor degreecategorylife, physical, and social science occupationsreference53367job details job summary: The QC Scientist I•Raw Materials will be accountable for executing and troubleshooting a variety of laboratory test methods, defining the requirements for implementation of procedures, processes and assays within QC, and identifying and implementing continuous improvement initiatives related to overall laboratory functionality.

location:

Westborough, Massachusetts job type: Contract salary: $50.00•57.65 per hour work hours: 9 to 5 education: Bachelors responsibilities: Execute and troubleshoot raw material testing in support of production activitiesPerform routine release sampling and managing testing of raw materials, such as compendial analysis per USP, Ph.

Eur., and JP monographs and general chapters, based on cGMP and internal proceduresDesign and perform testing in support of method transfer/validation/qualification/verificationReview/authorize data and perform analysis and interpretation of test results and trendsDesign and/or participate in method development; equipment qualification/validation studies; deviation and OOS investigationsPerform QC lab support activities including but not limited to sample management, reagent preparation, instrumentation maintenance, and instrument calibrationSupport and mentor junior team membersCollaborate with other network sites to share best practicesOther duties as required qualifications:

Required:

B.S. degree in chemistry, biological sciences or related field with 6+ years or M.S. degree with 4+ years of relevant experience in a GMP Quality Control rolePrior laboratory hands-on experience with a variety of techniques such as FTIR, Raman, Near-IR, HPLC analysis and other compendial assaysTechnical knowledge and experience in relevant areas of 21CFR, ICH, USP, Ph. Eur. and FDA guidance documents as well as cGXPs in support of clinical and commercial manufacturingProven knowledge in cGMP raw material program (RM sampling plans and testing requirements)Ensures inspection, testing and release timelines are met.

Strong understanding of data integrity requirements and regulatory requirements pertaining to biotechnology and pharmaceutical industries and proven experience analyzing experimental dataExperience using LIMS as an end user; Excellent technical writing and verbal communication skillsMust be capable of observing and adhering to lab safety standards and proceduresSuccessfully performs work independently with minimal instructionsStrong interpersonal skills, highly collaborative within a multi-discipline team and contributes to a supportive and positive work environment, strong knowledge of GMP, SOPs and quality control processes, and strong knowledge of quality systems and regulatory requirementsExcels in a fast-paced team environment, handles multiple tasks concurrently, and in a timely fashionHighly self-motivated and goal orientedWill support and demonstrate quality standards to ensure data of highest quality and works closely with team and other functional key stakeholders on the Astellas Operations team to execute work and will be expected to perform other duties and/or special projects as assigned

Preferred:

Experience in a Biotech/Pharmaceutical company with a high growth, fast-paced environmentExperience in qualification of analytical equipment, including those with computerized systemsExperience in method validation/qualification/verification/transfer

Working Conditions:

This role frequently requires long periods of sitting, standing and use of hands and regular motion to include bending, stooping, and lifting up to 20lbs.

This is an on-site role working in a cGMP regulated manufacturing facility. #LI-AM1 skills: SOP, Laboratory Information Management Systems (LIMS), Flow Cytometry, GMP (Good Manufacturing Practice), High Pressure Liquid Chromatography (HPLC),

Raw Materials 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. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.