Sr. Specialist, QA, Site Based, Redmond, WA
Evotec(7 days ago)
About this role
The Senior QA Specialist at Evotec Biologics is responsible for ensuring compliance with cGMP standards and overseeing document control activities in a biopharmaceutical environment. The role involves managing and issuing controlled documents, supporting audits, and collaborating across functional areas to maintain quality standards.
Required Skills
- document Control
- cGMP
- Quality Assurance
- Audit Support
- Document Management
- Labeling
- Reconciliation
- CAPA
- Regulatory
- Biopharmaceutical
Qualifications
- Bachelor’s Degree in biological or engineering science
About Evotec
evotec.comEvotec is a global biotechnology company committed to advancing drug discovery & development together with our partners for medicines that matter.
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