Instrumentation Specialist

pfizer.de

Andover, Massachusetts, US
Base: $82,700.00 - $137,900.00; bonus/equity: 10.0...
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Instrument lifecycle project work
Cgmp instrument support
Quality control laboratory support
** Pfizer is seeking an Instrumentation Specialist for its Andover, MA site to drive instrumentation lifecycle activities in support of Quality Control Laboratory and Production Operations. The ideal candidate will have relevant experience in a regulated environment, particularly within the pharmaceutical industry, and will engage in various projects involving instrument validation, maintenance, and troubleshooting. **

Job Summary

  • The Instrumentation Specialist drives instrumentation lifecycle activities in support of the Quality Control Laboratory and Production Operations Instrument Program(s).
  • In this role, you will support the Instrument Lifecycle Program and validation, maintenance, and decommissioning projects, and lead project management and technical support across instrumentation processes.
  • The position offers a competitive salary range, eligibility for a bonus, and comprehensive benefits including a 401(k) plan, paid time off, and health coverage.

Matching Summary

Match Score: 75

** Pfizer is seeking an Instrumentation Specialist for its Andover, MA site to drive instrumentation lifecycle activities in support of Quality Control Laboratory and Production Operations. The ideal candidate will have relevant experience in a regulated environment, particularly within the pharmaceutical industry, and will engage in various projects involving instrument validation, maintenance, and troubleshooting. **

Salary

Base: $82,700.00 - $137,900.00; Bonus/Equity: 10.0% bonus target; Benefits: Comprehensive benefits package including 401(k), paid time off, health, dental, and vision coverage

Skills & Requirements

Must-have

  • Instrument lifecycle project work
  • cGMP instrument support
  • Quality Control Laboratory support
  • Production Operations support
  • Instrument maintenance programs
  • Electronic data reconciliation

Nice-to-have

  • Continuous improvement culture
  • Cross-functional team collaboration
  • Adapt to changing priorities
  • Self-motivated project tracking

Key Requirements

  • Bachelor's degree with 2 years of experience OR Master's degree with 0+ years of experience OR Associate's degree with 6 years of experience OR High school diploma with 8 years of experience
  • cGMP pharmaceutical/biopharmaceutical industry experience
  • Experience supporting instrument lifecycle processes in a regulated environment
  • Permanent work authorization in the United States

Work Rights

Permanent work authorization required

Tailored Resume

Cover Letter