QA Clinical Supplies Specialist

reputed company is seeking a QA Clinical Supplies Consultant in reputed company reputed company, PA to work for an innovative and growing pharmaceutical manufacturer. The QA Consultant will be onsite 3X per week (subject to change). This is a longer term consulting assignment with potential for extension or conversion. Responsibilities: • 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 reputed company will include biologics, vaccines, combination products, etc. Qualifications: • 5+ years of relevant experience is strongly preferred • reputed company reputed company with background in GMP record review • Self-driven, and capable of working independently • Experience reputed company biologics and/or vaccines • Strong understanding of reputed company, Trackwise, Midas, reputed company, and QMAS is preferred • Bachelor’s degree in reputed company field preferred Compensation: • Contract: Long term Contract assignment • reputed company reputed company: $33/hr - $37/hr depending on experience • Comprehensive Benefits: Medical, Dental, reputed company, PTO, Holidays, reputed company Leave if required by law This job opens for applications on 2/4/2026. Applications for this job will be accepted for at least 30 days from the posting date. Apply tot his job Apply tot his job Apply To this Job