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Pfizer is seeking a Validation Engineer I to support the qualification of manufacturing processes and equipment in compliance with GMP standards. This hybrid role requires a degree or relevant experience and includes responsibilities such as coordinating validation activities, performing temperature mapping, and managing validation documentation.
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Job Summary
This role will provide validation support related to qualification of manufacturing processes and equipment used for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio.
Responsibilities include coordinating and executing validation deliverables, supporting IQ/OQ/PQ activities, managing validation schedules, and reviewing and completing validation documentation.
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: 75
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Pfizer is seeking a Validation Engineer I to support the qualification of manufacturing processes and equipment in compliance with GMP standards. This hybrid role requires a degree or relevant experience and includes responsibilities such as coordinating validation activities, performing temperature mapping, and managing validation documentation.
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Salary
Base: $68,600.00 - $114,300.00; Bonus/Equity: 7.5% of base salary; Benefits: Comprehensive benefits package including 401(k), paid time off, medical, dental, vision