Location: San Diego, CA
Department: Azzur San Diego, LLC
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Department: Azzur San Diego, LLC
Job Description
3-10 years validation experience. Must have analytical instruments qualification experience. CSV for analytical instruments preferred.
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- 3-10 years’ experience in validation services in a regulated, manufacturing environment within the biotechnology, pharmaceutical, or cell and gene therapy
- Hands on experience in executing C&Q protocols for QC lab equipment and processes.
- Experience in Computer System Validation for lab instruments is desired
- Strong knowledge of FDA, EU and cGMP regulations and good documentation practices
- Ability to create all validation lifecycle documetns
- Proficient in Microsoft Word, Excel, PowerPoint
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