Base: $90,816-$126,991; bonus: target 10% of base ...
5+ years cgmp facility experience
Iq oq pq protocol generation and execution
Validation master plan preparation
The role involves overseeing the development of new and improved processes for the economical and safe manufacture of experimental and bulk active-drug materials
Job Summary
The role involves overseeing the development of new and improved processes for the economical and safe manufacture of experimental and bulk active-drug materials.
Candidates will manage the preparation and approval of validation protocols for critical equipment while ensuring compliance with formulation specifications.
The position offers a comprehensive benefits package including medical, dental, vision, life insurance, disability, and a 401(k) plan with company contributions.
Matching Summary
The role involves overseeing the development of new and improved processes for the economical and safe manufacture of experimental and bulk active-drug materials.
Salary
Base: $90,816-$126,991; Bonus: Target 10% of base salary; Benefits: Comprehensive health, 401(k), paid time off
Skills & Requirements
Must-have
5+ years cGMP facility experience
IQ OQ PQ protocol generation and execution
Validation Master Plan preparation
Aseptic and terminal sterilization operations
Equipment troubleshooting and change control
Nice-to-have
Statistical analysis tools proficiency
Strong leadership and communication skills
Experience with outside customer coordination
Key Requirements
Minimum 4-year degree in Science or Engineering
5+ years related experience in a cGMP facility
Knowledge of cGMPs, industry guidance, and aseptic techniques