Supplier Quality Senior Specialist

Role: Senior Supplier Quality Specialist supporting GMP/GDP vendor and material management at Bristol Myers Squibb's biologics site. Responsibilities: qualify and manage vendors, oversee lifecycle of starting materials for biologics production, handle change notifications, and address non-conformance issues through deviations, SCARs, and CAPAs. Review and approve technical documents, collaborate with site stakeholders, and support audits. Qualifications: B.S. in science, engineering, biochemistry, or related field; minimum 4 years' experience in regulated biopharma environments; deep knowledge of US/EU cGMP regulations, ISO standards, and electronic systems like SAP, Veeva, Syncade. Skills: attention to detail, accountability, strong communication, and collaborative mindset. High-value specifics: biologics manufacturing, GMP/GDP compliance, vendor qualification, lifecycle management of raw materials, change control, and GxP oversight. Work setup: onsite at Devens, MA, with required presence per occupancy type; no travel specified.