CSV Specialist
Siegfried(19 days ago)
About this role
The role involves leading and supporting validation activities for computerized systems used in a pharmaceutical manufacturing environment. The specialist ensures compliance with quality standards and supports system configuration, validation, and audits in a GMP setting.
Required Skills
- Validation
- cGMP
- Laboratory Systems
- Data Integrity
- System Configuration
- Regulatory Compliance
- Validation Protocols
- SOPs
- Laboratory Equipment
- Audit Support
About Siegfried
siegfried.chSiegfried is your trusted global CDMO partner. Offering development and manufacturing from early-phase to commercial, from drug substance to drug product.
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