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.
• The annual base salary for this position ranges from $68,600.00 to $114,300.00, eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary.

Matching Summary

Salary

Base: $68,600.00 - $114,300.00; Bonus/Equity: 7.5% bonus target; Benefits: Comprehensive and generous benefits package

Skills & Requirements

Key Requirements

• Bachelor's degree with 0+ years experience
• Associate's degree with 4 years experience
• High school diploma with 6 years experience
• Experience in GMP biotechnology manufacturing
• Execute against Standard Operating Procedures
• Document entries in compliant manner

Work Rights