Instrumentation Specialist

pfizer.hu

Andover, Massachusetts, USA
Base: $82,700.00 - $137,900.00; bonus/equity: 10.0...
Hybrid
Instrument lifecycle activities
Cgmp instruments
Quality control laboratory support
Pfizer is seeking an Instrumentation Specialist to support the Quality Control Laboratory and Production Operations at its Andover, Massachusetts site. The successful candidate will oversee instrumentation lifecycle activities, facilitate project management, and ensure compliance with cGMP standards

Job Summary

  • The Instrumentation Specialist drives instrumentation lifecycle activities in support of the Quality Control Laboratory and Production Operations Instrument Program(s) at the Andover, Massachusetts site.
  • In this role, you will support the Instrument Lifecycle Program and validation, maintenance, and decommissioning projects, and lead/provide project management and technical support across instrumentation processes.
  • We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.

Matching Summary

Match Score: 85

Pfizer is seeking an Instrumentation Specialist to support the Quality Control Laboratory and Production Operations at its Andover, Massachusetts site. The successful candidate will oversee instrumentation lifecycle activities, facilitate project management, and ensure compliance with cGMP standards.

Salary

Base: $82,700.00 - $137,900.00; Bonus/Equity: 10.0% target; Benefits: Comprehensive and generous benefits package

Skills & Requirements

Must-have

  • Instrument lifecycle activities
  • cGMP instruments
  • Quality Control Laboratory support
  • Production Operations support
  • Instrument maintenance programs
  • Troubleshooting instrumentation issues

Nice-to-have

  • Continuous improvement culture
  • Adapt to rapidly changing priorities
  • Work collaboratively on a cross-functional team
  • Self-motivated project tracking

Key Requirements

  • Bachelor's degree with 2 years experience OR Master's degree with 0+ years experience OR Associate's degree with 6 years experience OR High School diploma with 8 years 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