QA Documentation Specialist
(m/f/d)
Freelance/temporary employment for a project Neuchatel Start date: asap Reference number: 838947/1
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Responsibilities
1. Own and maintain documentation systems and archiving processes
2. Provide user support and training on documentation tools (, Veeva Vault)
3. Create, update, and manage controlled documents
4. Collaborate On site and global initiatives to improve quality systems
5. Support audits, inspections, and quality metrics reporting.
Profile
6. Degree in life sciences or related field
7. Experience in the (bio)pharma industry
8. Knowledge of GMP, GDDP, and regulatory standards
9. Fluent in French and English
10. Proficient in Microsoft Office and document management systems.
Benefits
11. Good infrastructure
12. A very renowned company