# Manager, CSV Cell Therapy

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

Canonical page: https://career.thegoodapps.co/jobs/b8babcb4-aa0b-4954-acd3-8a499bc14e63

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

- Employment type: full time
- Seniority: Mid
- Location: Summit, NJ
- Salary: 106630 – 129214 USD per year

## Summary

This role leads equipment validation and computerized system management for a cell therapy manufacturing site, overseeing both technical execution and team development. It suits experienced pharmaceutical professionals who combine hands-on qualification expertise with supervisory capability and a grasp of FDA compliance requirements.

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

## Skills named

Microsoft Office, Microsoft Visio, SDLC Software Development Life Cycle, Technical Writing

## Required

- Bachelor's degree or equivalent experience
- Minimum 5 years in FDA-regulated industry
- Strong understanding of cGXP and good documentation practices
- Working knowledge of ISPE guidance and 21 CFR Part 11
- Working knowledge of SDLC principles
- Ability to document User and Functional Requirements
- Knowledge of pharmaceutical laboratory and manufacturing systems
- Experience executing equipment qualification documents
- Ability to interact with manufacturing, QA, and Facilities teams
- Strong MS Windows knowledge
- Ability to manage multiple concurrent tasks
- Strong written and verbal communication skills
- Proficiency in Microsoft Office Suite
- Hands-on leadership of direct reports

## Nice to have

- Experience with pharmaceutical laboratory and manufacturing systems implementation
- Research and development of validation tools and solutions
- Standardization and review of validation deliverables

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Summit-West---NJ---US/Manager--CSV-Cell-Therapy_R1604099