About this role
Role Overview
- Execution of day-to-day QA responsibilities for GMP manufacturing
- Building and enhancing quality assurance systems
- Review and assess quality events of eQMS
- Develop, review, and deliver training regarding QMS process or system changes
- Support QA QMS in internal and external audits and regulatory inspections
- Monitor and review effectiveness for QMS through trending, analysis, and metrics
Requirements
- Bachelor’s degree in biological or engineering science
- Minimum of 3 years relevant experience in a biopharmaceutical/Pharmaceutical cGMP manufacturing or similar environment
- Ability to collaborate and communicate cross-functionally
- Proven attention to detail
Benefits
- Discretionary annual bonus
- Comprehensive benefits including Medical, Dental, and Vision
- 401k company match
- Flexible paid time off
- Paid holidays
- Wellness benefits
- Transportation benefits