Manager, Csv - Equipment And Instrumentation

Bristol Myers Squibb UK

Base: $106,630 - $129,214; bonus/equity: + incenti...
Hybrid (50% onsite)
Cgmp requirements
Good documentation practices
Ispe guidance
Bristol Myers Squibb is seeking a Manager for CSV - Equipment and Instrumentation in the Cell Therapy sector, responsible for managing the implementation and qualification of laboratory and manufacturing equipment. The role requires strong analytical skills and a deep understanding of regulatory compliance within the pharmaceutical industry

Job Summary

  • The Manager, CSV Equipment and Instrumentation - Cell Therapy supports the successful implementation and support of manufacturing and laboratory equipment and local benchtop/standalone computerized systems.
  • This individual carries out routine tasks and functions, and uses strong analytical skills to recognize and solve common problems of various degrees of complexity and scope.
  • Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment and offers a wide variety of competitive benefits, services and programs.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Manager for CSV - Equipment and Instrumentation in the Cell Therapy sector, responsible for managing the implementation and qualification of laboratory and manufacturing equipment. The role requires strong analytical skills and a deep understanding of regulatory compliance within the pharmaceutical industry.

Salary

Base: $106,630 - $129,214; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • cGMP requirements
  • good documentation practices
  • ISPE guidance
  • 21 CFR Part 11
  • Data Integrity compliance
  • SDLC principles
  • pharmaceutical laboratory and manufacturing systems
  • equipment qualification documents
  • MS Windows client and server technologies
  • technical writing and document development

Nice-to-have

  • productive, learning environment
  • building trust and collaborative relationships
  • innovate, research and develop tools

Key Requirements

  • BS degree or equivalent experience
  • Minimum 5 years of experience in FDA-regulated industry
  • at least 2 years of recent hands-on CSV and implementation experience

Work Rights

Not specified

Tailored Resume

Cover Letter