Job Summary
A company is looking for a Senior Quality Associate.
Key Responsibilities
- Author and review Standard Operating Procedures (SOPs)
- Provide Quality Onboarding training and support vendor management activities
- Assist in compiling metrics for Quality Management Review and support quality performance/continuous improvement activities
Required Qualifications
- Bachelor's degree in Biology, Chemistry, or a relevant scientific discipline preferred
- 3-5 years of full-time cGMP Quality Assurance experience
- Experience with eQMS (e.g., ACE, TrackWise)
- Working knowledge of current industry practices and standards in an FDA-regulated biotechnology company
- Experience working with CDMOs preferred
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