The role involves leading and participating in critical document reviews and ensuring compliance with cGMPs across manufacturing and support areas
Job Summary
The role involves leading and participating in critical document reviews and ensuring compliance with cGMPs across manufacturing and support areas.
The position requires providing technical guidance, managing investigations, audits, and CAPAs, and supporting product transfers to maintain quality standards.
FITS LLC is a flexible, family-oriented service provider focused on employee well-being while delivering top-quality talent to the Pharmaceutical, Medical Device, and Manufacturing industries.
Matching Summary
The role involves leading and participating in critical document reviews and ensuring compliance with cGMPs across manufacturing and support areas.
Skills & Requirements
Must-have
Quality Assurance & cGMP Compliance
GMP Document Approval
Investigation & Root Cause Analysis
Cross-Functional Collaboration
Bilingual English & Spanish
Nice-to-have
Customer service oriented
Innovative and proactive mindset
Team collaboration and coaching
Flexible shift availability
Key Requirements
Bachelor's Degree in Chemical Engineering, Biology, or Microbiology Science
Six years experience in Pharmaceutical Manufacturing