QA Clinical Supplies Specialist (Hybrid Schedule)
📋 Role Overview & Responsibilities
Piper Companies is currently looking for an experienced QA Clinical Supplies Specialist in Rahway, NJ to work for an innovative and growing pharmaceutical manufacturer.
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 Clinical 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
5+ years of relevant experience is strongly preferred 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
Pay Commensurate on experience 1 Year Contract with possible extension Comprehensive Medical benefits: Medical, Dental, Vision, 401K
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
Frequently Asked Questions
How do I apply for the QA Clinical Supplies Specialist (Hybrid Schedule) position at Piper Companies? ▼
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Is this position eligible for remote work or visa sponsorship? ▼
This position is located in Rahway, NJ with potential relocation and sponsorship assistance depending on candidate qualifications.
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