Regulatory Jobs
Hero Gradient Background
Bristol Myers Squibb's glass research building at Cambridge Crossing with the Boston skyline behind it
Bristol Myers Squibb logo

New · posted Oct 21

Bristol Myers Squibb · Biotechnology

Manager, Supplier Quality

  • Indianapolis, IN +1 more
  • Hybrid
  • Full-time
  • Manager
Save
Pay$124K–$151Ka year · employer provided
EmploymentFull-time
LocationIndianapolis, IN +1 moreHybrid
LevelManager
FunctionQuality AssuranceQuality
Deadline

Closes Nov 6, 2026 · 15 days left

The role

The Manager for Supplier Quality will be responsible for ensuring supplier activities are in compliance with RayzeBio policies, standards, procedures and global cGMPs to support commercial and clinical operations.  In addition, the role will provide leadership of material lifecycle management, qualification, change management, non-conformance, and continuous improvement.

What you need

  • At minimum, a bachelor's degree in engineering or a life or physical science related field (including biology, biochemistry, chemistry) is required. 

  • Minimum 5 years of work experience in Quality Assurance

  • Experience in managing the quality of suppliers providing raw materials, consumables and services for finished product manufacturing is highly preferred. Experience with material lifecycle management is highly preferred.  Familiarity with Quality Risk Management principles is valuable.

  • Familiarity with SAP is valuable.

  • Knowledge of US, EU and rest-of-world cGMP regulations and guidance.

  • Demonstrated leadership, interpersonal, communication, and motivation skills.

  • Excellent writing and oral communication skills are required.

  • Previous work responsibility, which required a high degree of attention to detail.

  • Well-practiced in exercising sound judgment in decision-making.

  • Demonstrated prioritization and organization skills.

Skills named in this posting

What you'll do

Essential duties and responsibilities include the following.  Other duties may be assigned as required.

  1. Oversees the qualification and management of Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) vendors. This includes identifying and assessing new vendors, developing and revising Quality Agreements, and maintaining the Approved Vendor List.

  2. Manages site implementation of material qualification, vendor change notification, and material non-conformance programs.

  3. Manage the lifecycle of materials used for the manufacture of starting materials, drug substance, and drug products, which involves material qualification, maintenance, and reduced testing. 

  4. Provides oversight and review of supplier complaints and responses

  5. Conduct quality assessment of supplier change notifications and ensure actions are driven to completion utilizing change management programs.

  6. Support the external supplier audit program as a team member and/or lead auditor. Ensure that suppliers have quality and production systems that meet applicable regulatory, cGMP and RayzeBio requirements. Evaluate observation responses, track responses and follow up actions to closure.

  7. Handle discrepancy reporting, deviations and Corrective and Preventive Actions (CAPA) related to nonconforming materials or services provided by vendors.

  8. Perform quality reviews and approvals for functional area documents, including Standard Operation Procedures (SOPs), technical documents, reports, agreements, qualifications, and various forms.

  9. Establishes and implement processes to ensure quality oversight of on-site service vendors, collaborating closely with Facilities & Engineering, MS&T, and QA Operations.

  10. Coordinate and lead meetings with site stakeholders, other network sites, and external partners to execute vendor and material management programs, including discussions, negotiations, and dispute resolution.  

  11. Lead the team in cross-functional meetings and initiatives concerning supplier and material activities.

  12. Participates as a core team member in any corporate or health authority inspections.

  13. Identifies and reports discrepancies from required work practices or procedures to management.

  14. Makes sound decisions by exercising judgment within generally defined practices and policies and applies appropriate notification to management as appropriate.

  15. Leads teams and cross-functional project teams and drives team performance and results. Contributes highly to departmental performance and quality initiatives; able to conceptualize impact of Quality initiatives in terms of cross-functional teams.

  16. Applies AI to improve team execution and decision‑making

  17. Other QA specific responsibilities as assigned by QA management

Pay

$124,449 – $150,803 a year

Employer provided
How this compares

Compensation Overview

Indianapolis - RayzeBio - IN: $124,449 - $150,803 Remote - United States - US: $124,449 - $150,803

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans – including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).

U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.

Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.

Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.

U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits

Where you'll work

Indianapolis, IN +1 moreHybridOpen in Maps (opens in a new tab)

Also posted for: Remote (US)

More jobs in Indianapolis, IN +1 more

Working conditions

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and distance vision.

This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials.

The position may require occasional travel, but not more than 5%.

The noise level in the work environment is usually moderate.

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

A team of smiling Bristol Myers Squibb colleagues cheering as a coworker stacks cups in an office game

From the posting

About Bristol Myers Squibb

Life at BMS

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/

RayzeBio and Bristol Myers Squibb

RayzeBio was acquired by Bristol Myers Squibb (BMS) in 2024 and is a wholly-owned subsidiary of BMS; however, RayzeBio will continue to operate as a standalone organization.

Bristol Myers Squibb company page · 50 open roles
Equal opportunity, accessibility and legal noticesBristol Myers Squibb's statements, word for word

Supporting People with Disabilities

BMS and RayzeBio are dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS and RayzeBio will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

For roles based in Los Angeles County only:  If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

If this posting is missing required information required by local law or incorrect, contact BMS at [email protected] with the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.

R1600401 : Manager, Supplier Quality

Job intelligence

The context around this role

Live data · October 23, 2026

Salary intelligence

How the pay compares

This role's midpoint is 10% below the US median for Quality Assurance roles at this level.

This roleEmployer provided

$124,449 to $150,803 a year

Manager roles in the US111 roles publishing pay

Middle half $132,000 to $167,500, median $153,000
Annual base pay
Annual base payLowMedianHigh
This role$124,449—$150,803
All US$132,000$153,000$167,500

This role: Bristol Myers Squibb's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 23, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 927 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Bristol Myers Squibb's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $81K median251 open

  2. One step back

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $119K median394 open

  3. This role

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $153K median144 open

  4. Next step

    Director

    Often: Director, Quality · Associate Director, Quality Assurance

    $209K median121 open

  5. Later

    VP & Executive

    Often: AVP · DX Head of Regions Quality Management and Regulatory Affairs

    $302K median17 open

Career resources on Quality Assurance

Skills DNA

What this role leans on

How many of the posting's 29 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 5 linesLab testing and methods: 1 lineDocumentation and SOPs: 4 linesInvestigations and CAPA: 4 linesValidation and qualification: 4 linesRegulatory submissions: 1 lineQuality systems and risk: 6 linesData and digital systems: 1 lineCollaboration and leadership: 10 linesGMPLab testingDocumentationInvestigationsValidationSubmissionsQuality systemsData systemsTeamwork
  • Collaboration and leadership10
  • Quality systems and risk6
  • GMP and compliance5
  • Documentation and SOPs4
  • Investigations and CAPA4
  • Validation and qualification4
  • Lab testing and methods1
  • Regulatory submissions1
  • Data and digital systems1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

From Regulatory News

Manufacturing and quality coverage for this profession

Company hiring pulse

Bristol Myers Squibb on Regulatory Jobs

50
Open roles
48
Distinct roles
10
Locations

By discipline

  • Quality42 84%
  • Regulatory8 16%

By level

  • Senior & Principal19 38%
  • Associate & Specialist12 24%
  • Manager10 20%
See all 50 Bristol Myers Squibb roles

More roles at Bristol Myers Squibb

All 50 Bristol Myers Squibb roles

Similar Quality Assurance roles elsewhere

Manager, Supplier Quality at Bristol Myers Squibb

Applications close November 6. $124K–$151K a year, employer provided.

Job alerts