Batch Record Reviewer
(m/f/d)
Freelance/temporary employment for a project Visp Start date: asap Reference number: 841900/1
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Responsibilities
1. Investigate discrepancies such as failed process parameters or material consumption issues
2. Evaluate and clarify operator comments in batch records according to GMP and ALCOA+ standards
3. Collaborate with cross-functional teams to resolve batch record issues
4. Provide quality impact assessments for deviations and process failures
5. Use systems such as MES Syncade, DeltaV, Trackwise, SAP, LIMS, and DMS for data analysis
6. Support documentation tasks including lifecycle document authoring and cleaning report compilation
7. Ensure traceability and compliance in all documentation activities
8. Participate in internal and external discussions related to logistics and quality
9. Maintain accurate records of stock management, shipping preparation, and material receipt
Profile
10. Bachelor’s degree in Life Sciences or Biotechnology (preferred but not mandatory)
11. Prior experience in GMP-regulated environments is a plus
12. Hands-on experience in production, logistics, and batch record review
13. Familiarity with warehouse operations, including goods receipt and inventory control
14. Ability to work independently and meet deadlines with minimal supervision
15. Strong attention to detail and documentation accuracy
16. Proficient in using enterprise systems (SAP, LIMS, MES, etc.)
17. Fluent in German; English proficiency at B2 level
18. Forklift experience (R1 & R2) – informal training completed
19. Open to candidates without SUVA-recognized certification
Benefits
20. Opportunity to work with Lonza, a leading company in the life sciences industry
21. Gain experience in GMP and quality assurance processes
22. Collaborative work environment with cross-departmental exposure