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Validation Engineer
BachemQuality Engineer fulfilling GMP operations with cleaning validation and equipment qualification. Collaborating with Manufacturing and Engineering for process validation in pharmaceutical industry.
Posted 6/30/2026full-timeCalifornia • 🇺🇸 United StatesMid-LevelSenior💰 $84,274 - $115,877 per yearWebsite
About the role
Key responsibilities & impact- Support cleaning validation activities for API and PMO manufacturing
- Monitor facility / utility validated systems, plan, write and execute validation/ qualification protocols
- Conduct related investigations
- Train, coach and mentor team members
Requirements
What you’ll need- Bachelor’s degree in science discipline (chemistry, biochemistry, biology or equivalent)
- 5+ years of Commissioning, Qualification & Validation (CQV) / cleaning validation experience in a GMP/GDP environment
- Experience with planning, writing and executing qualification protocols (IQ, OQ, PQ) and reports
- Experience with validation / monitoring of critical pharmaceutical utility systems
- Understanding of cleaning validation requirements for pharmaceutical industry
Benefits
Comp & perks- competitive pay
- annual performance bonus
- comprehensive Medical/Dental/Vision coverage
- 401(k) plan with employer contribution
- paid vacation, personal and sick days
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
Cleaning ValidationCommissioningQualificationValidation ProtocolsExecution of Qualification ReportsMonitoring of Utility SystemsInvestigative AnalysisTraining and Mentoring
Soft Skills
CoachingTeam Leadership
Certifications
Bachelor’s Degree in Science Discipline