Aequor
Title:
Third Party Management Specialist
Location:
Framingham, MA
Duration:
Contract until July 2026 with possibility to extend
Shift:
Mon‑Fri 8:00‑4:30
The Third Party Management Specialist will oversee Third Party Quality operations for the MA BioCampus, ensuring excellence in quality standards and regulatory compliance across external partnerships. This role requires leading Supplier Change Notification (SCN) processes, managing third‑party quality event investigations, supporting quality agreement programs including periodic reviews and documentation, and collaborating cross‑functionally with QC, Facilities, and Manufacturing departments to resolve compliance issues. This position reports to the Head of Supplier Governance and requires the ability to gown and enter manufacturing/warehouse areas.
Qualifications
Minimum 6 years of quality/operations experience in a biotech/pharmaceutical cGMP manufacturing environment within an FDA‑regulated industry.
Bachelor's degree or equivalent experience in Supplier Quality.
Proficiency in Veeva quality management systems.
Strong knowledge of global pharmaceutical regulations (US, EU, Canada, Japan, Australia).
Expertise in material compliance from suppliers and vendors in a pharma/biotech/GMP manufacturing/FDA‑regulated environment.
Ability to gown and enter manufacturing/warehouse areas.
Nice to Have
Previous experience with Veeva, quality agreements, supplier compliance, supplier change notifications.
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Third Party Management Specialist
Location:
Framingham, MA
Duration:
Contract until July 2026 with possibility to extend
Shift:
Mon‑Fri 8:00‑4:30
The Third Party Management Specialist will oversee Third Party Quality operations for the MA BioCampus, ensuring excellence in quality standards and regulatory compliance across external partnerships. This role requires leading Supplier Change Notification (SCN) processes, managing third‑party quality event investigations, supporting quality agreement programs including periodic reviews and documentation, and collaborating cross‑functionally with QC, Facilities, and Manufacturing departments to resolve compliance issues. This position reports to the Head of Supplier Governance and requires the ability to gown and enter manufacturing/warehouse areas.
Qualifications
Minimum 6 years of quality/operations experience in a biotech/pharmaceutical cGMP manufacturing environment within an FDA‑regulated industry.
Bachelor's degree or equivalent experience in Supplier Quality.
Proficiency in Veeva quality management systems.
Strong knowledge of global pharmaceutical regulations (US, EU, Canada, Japan, Australia).
Expertise in material compliance from suppliers and vendors in a pharma/biotech/GMP manufacturing/FDA‑regulated environment.
Ability to gown and enter manufacturing/warehouse areas.
Nice to Have
Previous experience with Veeva, quality agreements, supplier compliance, supplier change notifications.
#J-18808-Ljbffr