Senior Specialist, Validation Engineer Ii

Bristor Myers Squibb

Devens, MA, United States
Base: $92,540 - $112,136; bonus/equity: + incentiv...
On-site
Develop and execute validation/qualification deliverables
Support equipment qualification and validation activities
Adhere to change management process
Bristol Myers Squibb is seeking a Senior Specialist, Validation Engineer II to support the qualification and validation of manufacturing and laboratory equipment at their Devens, MA facility. The role requires a minimum of 3 years of relevant experience, with a focus on regulatory compliance and maintaining equipment systems in a qualified state

Job Summary

  • The Senior Specialist, Validation Engineer II supports the successful implementation of manufacturing, and laboratory equipment alongside facilities and utilities.
  • Responsibilities include execution of validation lifecycle maintenance that includes establishment of validation document hierarchy, tracking execution work arising from change controls, shutdown/changeover management related to validation, and management of the revalidation and cleaning monitoring programs.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Specialist, Validation Engineer II to support the qualification and validation of manufacturing and laboratory equipment at their Devens, MA facility. The role requires a minimum of 3 years of relevant experience, with a focus on regulatory compliance and maintaining equipment systems in a qualified state.

Salary

Base: $92,540 - $112,136; 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

  • Develop and execute validation/qualification deliverables
  • Support equipment qualification and validation activities
  • Adhere to change management process
  • Familiarity with cGMP
  • Knowledge of regulatory validation requirements

Nice-to-have

  • Promote excellent customer service
  • Contribute to multi-function teams
  • Represent department before regulatory agencies
  • Working understanding of lean principles

Key Requirements

  • Minimum of 3+ years relevant experience
  • Minimum of 2+ years’ experience in equipment, facility, or utility qualification
  • Bachelor of Science degree in Chemical Engineering, Mechanical Engineering, or related discipline

Work Rights

Not specified

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