Baxter Healthcare is seeking a Manufacturing Validation Associate II to support hands-on validation activities in a GMP manufacturing environment. The ideal candidate will have relevant experience with validation processes and regulatory compliance, and the position offers a competitive salary and comprehensive benefits
Job Summary
This role is primarily focused on hands-on validation activities for manufacturing equipment, processes, utilities, and facilities within an onsite GMP manufacturing environment.
The position supports the development and execution of validation deliverables related to equipment qualification, process validation, cleaning validation, and utilities/facility validation for commercial manufacturing operations.
Baxter offers comprehensive compensation and benefits packages including medical and dental coverage starting day one, 401(k) matching, and paid time off ranging from 20 to 35 days based on length of service.
Matching Summary
Match Score: 85
Baxter Healthcare is seeking a Manufacturing Validation Associate II to support hands-on validation activities in a GMP manufacturing environment. The ideal candidate will have relevant experience with validation processes and regulatory compliance, and the position offers a competitive salary and comprehensive benefits.
Salary
Base: $88,000 - $121,000 annually; Bonus/Equity: Eligible for discretionary bonuses; Benefits: Comprehensive health, dental, 401(k) match, ESPP, and 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 knowledge application
Nice-to-have
Design of experiments DOE experience
Statistical software proficiency
Strong project management skills
Cross-functional team collaboration
Computerized system validation support
Key Requirements
BS Degree in Science, Engineering or Math with 2+ years experience
Direct hands-on experience writing and executing validation protocols
Must not be allergic to Cephalosporins or Penicillin
Ability to work at least 5 days onsite in the plant
Authorized to work for any employer in the U.S.
Work Rights
Must be authorized to work for any employer in the U.S.