QA Clinical Supplies
1 week ago
Responsibilities for the QA Clinical Supplies Specialist:
•Electronic batch record review of finished clinical goods to ensure clinical supplies are incompliance with cGMP and SOPs
•Check c linical supplier specifications, labeling, storage, etc.
•Review of Electronic records for regulatory submissions (IND or CTA)
•Areas of focus will include biologics, vaccines, combination products, etc.
Qualifications for the QA Clinical Supplies Specialist:
•2 + years of relevant experience in pharmaceutical/biotech industry or supply chain
•Quality mindset with background in GMP record review
•Self-driven, and capable of working independently
•Experience within biologics and/or vaccines
•Strong understanding of SAP, Trackwise, Midas, Veeva, and QMAS is preferred
•Bachelor's degree in related field preferred
Compensation for the QA Clinical Supplies Specialist:
•$38-46hr
•1-year contract with possible extension
•Medical, Dental, Vision, 401K, PTO
Keywords: clinical supplies, biologics, vaccines, electronic batch record review, batch record, cGMP, SOPs, specifications, labeling, regulatory submissions, SAP, Trackwise, Midas, Veeva, QMAS, QA, Quality Assurance
#LI-NW1 #LI-ONSITE
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