The Fountain Group
Third-Party QA Management Specialist
The Fountain Group, Framingham, Massachusetts, us, 01704
Currently I have an opening for a
Third-Party QA Management Specialist
located in
Framingham, MA.
Details for the position are as follows:
Job Description
The Third-Party Management Specialist will oversee Third Party Quality operations for the MA Bio-Campus, 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.
Collaborated cross-functionally with QC, Facilities, and Manufacturing departments to resolve compliance issues.
The ideal candidate will have a bachelor’s degree or equivalent experience in Supplier Quality, minimum 4+ years of Quality/Operations experience in a biotech/pharmaceutical cGMP manufacturing environment within an FDA-regulated industry.
Proficiency in Veeva quality management systems, and strong knowledge of global pharmaceutical regulations (US, EU, Canada, Japan, Australia).
Report to the Head of Supplier Governance and requires the ability to gown and enter manufacturing/warehouse areas.
Technical Information
Pay: $45-51 hourly (W2), depending on experience level
6-month contract, potential for extension or conversion
Onsite position, M-F, 8am-5pm
#J-18808-Ljbffr
Third-Party QA Management Specialist
located in
Framingham, MA.
Details for the position are as follows:
Job Description
The Third-Party Management Specialist will oversee Third Party Quality operations for the MA Bio-Campus, 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.
Collaborated cross-functionally with QC, Facilities, and Manufacturing departments to resolve compliance issues.
The ideal candidate will have a bachelor’s degree or equivalent experience in Supplier Quality, minimum 4+ years of Quality/Operations experience in a biotech/pharmaceutical cGMP manufacturing environment within an FDA-regulated industry.
Proficiency in Veeva quality management systems, and strong knowledge of global pharmaceutical regulations (US, EU, Canada, Japan, Australia).
Report to the Head of Supplier Governance and requires the ability to gown and enter manufacturing/warehouse areas.
Technical Information
Pay: $45-51 hourly (W2), depending on experience level
6-month contract, potential for extension or conversion
Onsite position, M-F, 8am-5pm
#J-18808-Ljbffr