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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
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Cleaning Validation and Commissioning, Qualification & Validation (CQV) within a GMP/GDP environment, with a strong focus on planning, writing, and executing qualification protocols. Capable of training and mentoring team members while ensuring compliance with pharmaceutical industry standards.
Highest-signal resume keywords
Cleaning Validation ExperienceCommissioning, Qualification & Validation (CQV)Qualification Protocols (IQ, OQ, PQ)GMP/GDP Environment ExperiencePharmaceutical Utility Systems Validation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Cleaning ValidationCommissioningQualificationValidation ProtocolsExecution of Qualification ReportsMonitoring of Utility SystemsInvestigative AnalysisTraining and Mentoring
Soft Skills
CoachingTeam Leadership
Certifications & Qualifications
Bachelor’s Degree in Science Discipline
Industry Keywords
GMPGDPPharmaceutical IndustryValidation Requirements
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