Role OverviewYou will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s commercial batches of drugs. You will ensure that product and process match the specifications based on established sampling and statistical process control procedures.
What You Will Do
Review and approve laboratory and manufacturing incidents and investigations. Collaborate in development and implementation of CAPA. Provide Quality Review and oversight of site cGXP documentation related to the support of manufacturing and Site/Engineering activities to ensure compliance with global regulatory agencies and Pfizer quality standards.
Why It Might Be a Fit
Ability to work in a fast-paced environment and be able and willing to juggle priorities as required. Exercises judgment in resolving moderate to complex quality issues. Plans and executes work independently and consult with supervisor as needed, providing a recommendation for a solution.
Requirements
- High school diploma with at least 10 years experience
- Associate’s degree with at least 8 years experience
- Bachelor’s degree with at least 4 years of experience
- Master’s degree with at least 2 years experience
- PhD with 0+ years of experience in GMP Pharmaceutical or Medical Device Manufacturing environment or relevant regulatory experience
Benefits
- 401(k) plan with Pfizer Matching Contributions
- Pfizer Retirement Savings Contribution
- paid vacation
- holiday and personal days
- paid caregiver/parental and medical leave
- health benefits to include medical, prescription drug, dental and vision coverage
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