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About the role
Key responsibilities & impact- Lead and guide moderately complex projects, managing time and resources effectively
- Make decisions to resolve moderately complex problems and develop new options guided by policies
- Manage external deviations in manufacturing and packaging processes
- Conduct quality reviews and report results to medical and quality groups
- Support the development of country quality strategic initiatives and leadership in quality issues
- Participate in internal cGMP audits and support regulatory inspections
Requirements
What you’ll need- Bachelor’s degree with at least 4 years of experience; OR a master’s degree with at least 2 years of experience; OR a PhD with 0+ years of experience; OR an associate’s degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience
- Substantial experience in pharmaceutical manufacturing and quality assurance.
- Experience with Current Good Manufacturing Practices (cGMP) and handling compliance issues.
- Knowledge of regulations related to vendor management programs and quality systems.
- Strong critical thinking skills and a proactive approach.
- Advanced computer skills in MS Office applications and a good understanding of enterprise systems such as SMS, eQMS, CoPilot.
Benefits
Comp & perks- 401(k) plan with Pfizer Matching Contributions
- Additional Pfizer Retirement Savings Contribution
- Paid vacation
- Holiday and personal days
- Paid caregiver/parental leave
- Paid medical leave
- Health benefits including medical, prescription drug, dental, and vision coverage
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
pharmaceutical manufacturingquality assuranceCurrent Good Manufacturing Practices (cGMP)compliance managementvendor managementquality systemscritical thinking
Soft Skills
leadershipproblem-solvingtime managementresource managementproactive approach
