

New · posted Oct 15
Bristol Myers Squibb · Biotechnology
Data Reviewer, Quality Control Microbiology
- Indianapolis, IN
- On-site
- Full-time
- Associate & Specialist
Closes Jan 1, 2027 · 79 days left
The role
RayzeBio is seeking a Quality Control Microbiology Data Reviewer, reporting to the Director- Microbiology Quality Control. The Data Reviewer will collaborate with the Radiation Safety Officer (RSO) to ensure laboratory compliance with the radiation safety program at the Indianapolis site. The position will require the applicant to work with and around ionizing radiation and hazardous chemicals.
The position will be located at RayzeBio’s manufacturing plant, in Indianapolis, IN.
Regarding work hours, we ask for candidates to be able to work a flexible schedule, including occasional weekend or off‑shift support based on business needs. This position is an on-site position.
What you need
- Bachelor’s degree (BS) in Microbiology, Biology, or a related life science discipline required.
- Minimum 3-5 years of experience in a QC Microbiology or related laboratory within a cGMP‑regulated environment.
- Experience supporting sterile manufacturing and/or radiopharmaceutical operations is highly desirable.
- Strong working knowledge of microbiological methods, EM programs, and regulatory expectations.
· Highly organized, detail‑oriented, and capable of managing multiple priorities in a fast‑paced environment.
· Strong knowledge of cGMP, USP <61>, <62>, <71>, <85>, EU GMP Annex 1, and data integrity principles.
· Ability to manage multiple review tasks under tight deadlines
· Effective communication skills — able to clearly document findings and interface with cross-functional teams
· Proactive in identifying process gaps and challenging the status quo to drive improvements
· Excellent written and verbal communication skills.
· Ability to work in classified cleanroom environments while wearing appropriate gowning.
· Uses AI tools to enhance individual productivity and quality of work
What you'll do
Essential duties and responsibilities include the following. Other duties may be assigned.
· Review and approve raw microbiological data including, but not limited to:
o Sterility testing o Bioburden testing o Endotoxin testing o Media qualification and growth promotion testing o Environmental Monitoring (viable air, surface, and personnel)
· Verify that out-of-specification (OOS), out-of-trend (OOT), and atypical results are properly identified, documented, and investigated
· Support microbiological investigations at the site.
· Ensure data is reviewed within defined timelines to support batch release and regulatory reporting
· Ensure all reviewed data meets cGMP, FDA, EMA, USP, and ICH requirements
· Support internal and external audits and inspections; serve as a subject matter expert for data review processes
· Author, review, and approve SOPs, batch records, protocols, and technical reports related to microbiological testing
· Compile and trend EM and microbiological data for periodic review reports and management review
· Identify data integrity issues and escalate appropriately in accordance with site procedures
· Partner with Production, Quality Assurance, Validation, and Regulatory Affairs teams to resolve data discrepancies and support investigations (e.g., CAPAs, deviation reports)
· Support method validation and qualification activities by reviewing generated data packages
· Identify non-value-add review steps and propose process improvements to streamline workflows and reduce cycle times
Pay
$82,236 – $99,650 a year
Employer providedCompensation Overview
Indianapolis - RayzeBio - IN: $82,236 - $99,650
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, INOn-siteOpen in Maps (opens in a new tab)
More jobs in Indianapolis, INWorking conditions
Regular interaction within office, warehouse, and manufacturing environments, with PPE required in certain areas.
Moderate noise levels.
Exposure to manufacturing, laboratory, and logistics environments.
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.

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.
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.
R1607426 : Data Reviewer, Quality Control Microbiology
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This role's midpoint is 52% above the US median for Quality Control roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US100 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $82,236 | — | $99,650 |
| All US (middle half) | $49,375 | $60,000 | $76,125 |
This role: Bristol Myers Squibb's own published range. Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 275 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Bristol Myers Squibb's own promotion track.
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.
- Lab testing and methods10
- Documentation and SOPs8
- GMP and compliance5
- Collaboration and leadership4
- Investigations and CAPA3
- Validation and qualification3
- Quality systems and risk2
- Data and digital systems2
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.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- European CommissionEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules and annexes
- USPUSP compendial chapters(official source, opens in a new tab)Bioburden (USP <61>), endotoxin (USP <85>), TOC (USP <643>) and water testing
Company hiring pulse
Bristol Myers Squibb on Regulatory Jobs
- 41
- Open roles
- 41
- Distinct roles
- 9
- Locations
By discipline
- Quality35 85%
- Regulatory6 15%
By level
- Senior & Principal18 44%
- Associate & Specialist9 22%
- Director7 17%
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Data Reviewer, Quality Control Microbiology at Bristol Myers Squibb
Applications close January 1. $82K–$100K a year, employer provided.

