Manager, Supplier Quality

Bristol Myers Squibb; Indianapolis (IN); On-site; USD 110,000 - 160,000; Full time

Job summary

RayzeBio in Indianapolis seeks a Manager of Supplier Quality to lead cGMP vendor activities and ensure material quality for clinical and commercial operations.

Responsibilities include vendor qualification, audits, change notifications, NCRs/CAPAs, document reviews, and cross-functional collaboration with occasional travel.

Qualifications

• Bachelor’s degree in engineering or life/physical sciences.
• Minimum 5 years in Quality Assurance with vendor/material quality in biopharma.
• Familiarity with cGMP regulations, SAP, and quality risk management.

Responsibilities

• Oversee qualification and management of GMP/GDP vendors.
• Manage material lifecycle including qualification, change control, non-conformance, and CAPAs.
• Lead supplier audits and evaluate change notifications.
• Handle discrepancy reporting and CAPAs.
• Review quality documents and coordinate with cross-functional teams.
• Participate in audits and inspections.
• Lead team initiatives and apply AI tools for process enhancement.

Skills

Vendor quality management

GMP compliance

Audit leadership

CAPA management

Cross-functional collaboration

AI in QA

Education

Bachelor’s degree in engineering or life/physical sciences

Tools

SAP

Job description

Role: Manager of Supplier Quality at RayzeBio, responsible for ensuring supplier activities comply with cGMP and RayzeBio standards to support clinical and commercial operations.

Core responsibilities

• oversee qualification and management of GMP/GDP vendors
• manage material lifecycle including qualification, change management, non-conformance, and continuous improvement
• lead supplier audits and evaluate change notifications
• handle discrepancy reporting and CAPAs
• review quality documents
• coordinate with cross-functional teams for vendor and material oversight
• participate in audits and inspections
• lead team initiatives and apply AI tools for process enhancement

Requirements

• bachelor’s degree in engineering, life or physical sciences
• at least 5 years in Quality Assurance, with experience managing raw material and vendor quality in biopharma
• familiarity with cGMP regulations, SAP, and quality risk management

Preferred

• experience with material lifecycle management
• supplier audits
• working within radiopharmaceutical or oncology sectors

Work setup

location in Indianapolis, with occasional travel (< 5%).