Description: It is a QA specialist position to provide QA support for the La Verne 2nd Formulation suite project. QA documentation review of validation protocols and final reports for the project as well as any other project related quality functions to ensure compliance to internal procedures as well as regulatory requirements.
QA review of validation protocols and final reports in support of routing requalification program.
- GMP experience and general understanding of quality systems.
- Understanding of Commissioning, Qualification, and Validation activities.
- Excellent attention to detail.
- Proficiency in generating and updating GMP documentation in Microsoft Word.
Nice to haves:
- Experience with the following quality document management systems:
- Veeva Vault