- Riverview, Michigan, United States
- On-site
- Full-time · Associate
- 1+ years
Support the implementation, execution, and maintenance of Quality Systems at the PPS-Riverview site to ensure compliance with FDA and international regulatory authorities.
Responsibilities
- Review batch production records to ensure GMP compliance
- Walk production areas to promote Good Manufacturing Practices
- Support QA administrative duties including issuing master production records
- Support internal and external audits and regulatory inspections
- Manage reports and documentation for audits and quality systems
Requirements
- Bachelor’s degree in the physical or biological sciences or engineering
- Associate’s degree with 2+ years experience in pharmaceutical operations
- 3-5 years experience in pharmaceutical operations or quality assurance