Randstad Life Sciences US
Associate II, Quality Control Chemistry
Randstad Life Sciences US, Norwood, Massachusetts, us, 02062
Recruiter - Life Sciences at Randstad USA
Contract – Potential to last up to 6 Months, to start
Norwood, MA
PR: $35-45/hour
Job Summary Step into a dynamic contract role as an Associate II, Quality Control Chemistry in Norwood, MA, with a pay rate of $35-$45/hour, focusing on essential analytical testing in a cGMP regulated environment. This position is ideal for a detail-oriented professional with a Bachelor's degree in a relevant scientific discipline and at least two years of experience in a pharmaceutical Quality Control laboratory. Core responsibilities include routinely performing in-process, release, and stability testing using a combination of analytical equipment such as HPLC, UPLC, DLS, and Karl Fischer. The role requires strict adherence to GDP for documenting results in LIMS and worksheets, and involves participation in lab investigations (OOS, OOT, OOE), troubleshooting, and assisting with inventory management and the review/writing of SOPs and protocols.
Job Responsibilities
Work on in-process, release and stability testing for raw materials, drug substance, intermediates, and drug products in accordance with cGMP, SOP, FDA, ICH and other regulatory requirements.
Routinely use analytical equipment including, but not limited to HPLC, UPLC, UV plate reader, particulate matter, particle size analysis with Dynamic Light Scattering, KF, Osmolality, etc.
Follow current test methods and/or protocols to perform analytical testing.
Document the testing procedure and results using Assay Performance Worksheets and/or LIMS as per GDP requirements and submit data packets for review
Maintain compliance to data integrity and cGMP in QC lab in line FDA and ICH guidance.
Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping and 5S activities, etc.
May assist with troubleshooting of assay methods and equipment.
Involved in lab investigations, OOS, OOT, OOE and deviation investigations.
May Implement CAPAs and perform effectiveness check.
Complete on job training activities
Help with inventory management of reference standards, reagents, supplies for testing
Review/write/revise SOPs, protocols and reports
Establish and maintain a safe laboratory working environment
Supports special projects as assigned
Additional duties as may be assigned
Education & Qualifications
BA/BS in relevant scientific discipline
At least two years in Quality Control laboratory in a pharmaceutical company
Previous experience with a combination of: HPLC, UPLC, UV, particle size analysis, DLS, Karl Fischer, Osmolality.
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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
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Norwood, MA
PR: $35-45/hour
Job Summary Step into a dynamic contract role as an Associate II, Quality Control Chemistry in Norwood, MA, with a pay rate of $35-$45/hour, focusing on essential analytical testing in a cGMP regulated environment. This position is ideal for a detail-oriented professional with a Bachelor's degree in a relevant scientific discipline and at least two years of experience in a pharmaceutical Quality Control laboratory. Core responsibilities include routinely performing in-process, release, and stability testing using a combination of analytical equipment such as HPLC, UPLC, DLS, and Karl Fischer. The role requires strict adherence to GDP for documenting results in LIMS and worksheets, and involves participation in lab investigations (OOS, OOT, OOE), troubleshooting, and assisting with inventory management and the review/writing of SOPs and protocols.
Job Responsibilities
Work on in-process, release and stability testing for raw materials, drug substance, intermediates, and drug products in accordance with cGMP, SOP, FDA, ICH and other regulatory requirements.
Routinely use analytical equipment including, but not limited to HPLC, UPLC, UV plate reader, particulate matter, particle size analysis with Dynamic Light Scattering, KF, Osmolality, etc.
Follow current test methods and/or protocols to perform analytical testing.
Document the testing procedure and results using Assay Performance Worksheets and/or LIMS as per GDP requirements and submit data packets for review
Maintain compliance to data integrity and cGMP in QC lab in line FDA and ICH guidance.
Performs general laboratory support activities including reagent preparation, sample management, equipment maintenance, lab housekeeping and 5S activities, etc.
May assist with troubleshooting of assay methods and equipment.
Involved in lab investigations, OOS, OOT, OOE and deviation investigations.
May Implement CAPAs and perform effectiveness check.
Complete on job training activities
Help with inventory management of reference standards, reagents, supplies for testing
Review/write/revise SOPs, protocols and reports
Establish and maintain a safe laboratory working environment
Supports special projects as assigned
Additional duties as may be assigned
Education & Qualifications
BA/BS in relevant scientific discipline
At least two years in Quality Control laboratory in a pharmaceutical company
Previous experience with a combination of: HPLC, UPLC, UV, particle size analysis, DLS, Karl Fischer, Osmolality.
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 health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
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