Supplier Quality Senior Specialist
Bristol Myers Squibb
August 17, 2026
Remote friendly (Devens, MA)
United States
Operations
Position Summary
The Supplier Quality Senior Specialist supports the GMP/GDP Vendor and Material Management programs at the Devens Biologics site, including vendor and material qualification/management, change management, and supplier non-conformance reporting and resolution.
Key Responsibilities
- Qualify and manage GMP/GDP vendors: assess vendors, create/revise quality agreements, maintain Approved Vendor List.
- Manage lifecycle of starting materials: material qualification/requalification, reduced testing, direct dispense.
- Assess supplier change notifications (SCN) and complete required actions in the BMS change management system.
- Support deviations, Supplier Corrective Action Requests (SCAR), and CAPA for nonconforming vendor materials/services.
- Review SOPs, technical documents/reports, agreements, qualifications, and forms.
- Oversee on-site service vendors in collaboration with business owners and QA Operations.
- Identify quality and business continuity risks and notify management as appropriate.
- Collaborate cross-functionally; may represent the team on supplier/material initiatives and support external audits.
Qualifications & Experience
- B.S. in science/engineering/biochemistry or related field (or equivalent education/experience/training).
- 4+ years in a regulated biopharmaceutical environment.
- Practical knowledge of US/EU cGMP and ISO standards.
- Familiar with SAP, Veeva, Syncade.
- Strong attention to detail, accountability, collaboration; excellent written/oral communication.
Compensation & Benefits (as stated)
- Devens, MA: $89,530–$108,490; additional incentive opportunities may apply.
- Health coverage; wellbeing programs; 401(k) and other insurance/disability/life benefits.
Application Instruction
- Apply even if the role doesn’t perfectly match your resume.
The Supplier Quality Senior Specialist supports the GMP/GDP Vendor and Material Management programs at the Devens Biologics site, including vendor and material qualification/management, change management, and supplier non-conformance reporting and resolution.
Key Responsibilities
- Qualify and manage GMP/GDP vendors: assess vendors, create/revise quality agreements, maintain Approved Vendor List.
- Manage lifecycle of starting materials: material qualification/requalification, reduced testing, direct dispense.
- Assess supplier change notifications (SCN) and complete required actions in the BMS change management system.
- Support deviations, Supplier Corrective Action Requests (SCAR), and CAPA for nonconforming vendor materials/services.
- Review SOPs, technical documents/reports, agreements, qualifications, and forms.
- Oversee on-site service vendors in collaboration with business owners and QA Operations.
- Identify quality and business continuity risks and notify management as appropriate.
- Collaborate cross-functionally; may represent the team on supplier/material initiatives and support external audits.
Qualifications & Experience
- B.S. in science/engineering/biochemistry or related field (or equivalent education/experience/training).
- 4+ years in a regulated biopharmaceutical environment.
- Practical knowledge of US/EU cGMP and ISO standards.
- Familiar with SAP, Veeva, Syncade.
- Strong attention to detail, accountability, collaboration; excellent written/oral communication.
Compensation & Benefits (as stated)
- Devens, MA: $89,530–$108,490; additional incentive opportunities may apply.
- Health coverage; wellbeing programs; 401(k) and other insurance/disability/life benefits.
Application Instruction
- Apply even if the role doesn’t perfectly match your resume.