# Senior Validation Engineer

Hiring organization: [Bristol Myers Squibb](https://career.thegoodapps.co/organizations/bristol-myers-squibb)

Canonical page: https://career.thegoodapps.co/jobs/9b72f723-bd09-45a5-9626-e8edcae98a79

Listed on Bristol Myers Squibb's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Senior
- Location: Indianapolis, IN
- Salary: 107904 – 130754 USD per year

## Summary

This role leads validation and commissioning efforts for a new radiopharmaceutical manufacturing facility, supporting the transition from construction through clinical and commercial operations. It suits experienced validation engineers who can independently manage complex GMP projects while mentoring others in a specialized biotech environment.

_Our summary, not Bristol Myers Squibb's wording._

## Skills named

Process Validation, Risk Management, Technical Writing

## Required

- BS or MS in a scientific field or equivalent work experience
- 4–8 years in radiopharmaceutical or injectable GMP manufacturing
- 4–8 years of validation experience in a GMP environment
- Technical writing skills
- Understanding of regulatory guidelines for validation and risk management
- Ability to work independently and with teams in a GMP cleanroom environment
- Willingness to handle radioactive materials

## Nice to have

- Experience with additional validation domains (process validation, QC assets, CSV, cleaning validation)
- Proficiency with AI tools to enhance productivity

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Indianapolis---RayzeBio---IN/Senior-Validation-Engineer_R1604602