Baxter is seeking a Manufacturing Validation Associate II to perform hands-on validation activities within a GMP manufacturing environment. The ideal candidate will possess a relevant degree, experience in validation protocols, and a strong understanding of regulatory requirements
Job Summary
The role focuses on hands-on validation activities for manufacturing equipment, processes, utilities, and facilities within an onsite GMP manufacturing environment.
Baxter is committed to equitable pay with a base salary range of $88,000 - $121,000 annually and offers comprehensive benefits including medical coverage starting day one.
Candidates must be authorized to work for any employer in the U.S. as sponsorship is not available for this position.
Matching Summary
Match Score: 85
Baxter is seeking a Manufacturing Validation Associate II to perform hands-on validation activities within a GMP manufacturing environment. The ideal candidate will possess a relevant degree, experience in validation protocols, and a strong understanding of regulatory requirements.
Salary
Base: $88,000 - $121,000 annually; Bonus/Equity: Eligible for discretionary bonuses; Benefits: Medical dental life insurance 401k matching paid time off
Skills & Requirements
Must-have
Hands-on validation activities in GMP environment
Equipment qualification IQ OQ PQ execution
Process validation PPQ protocol writing
Cleaning validation sampling and execution
FDA cGMP regulatory requirement application
Nice-to-have
Design of experiments DOE experience
Statistical software proficiency
Strong project management skills
Cross-functional team collaboration
Computerized system validation knowledge
Key Requirements
BS Degree in Science Engineering or Math with 2+ years experience
Master's Degree with 1+ years experience
Must not be allergic to Cephalosporins or Penicillin
Authorized to work for any employer in the U.S.
Ability to work at least 5 days onsite in the plant
Work Rights
Must be authorized to work for any employer in the U.S.