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Validation Specialist
vor 2 Monaten
Are you a seasoned Qualification Specialist looking for a new challenge in the pharmaceutical industry?
Hamlyn Williams is currently seeking a talented Validation Engineer to join our client, a leading pharmaceutical company in Germany, on a 12-month contract.
The successful candidate will be responsible for establishing, writing, updating, and archiving qualification documents according to the company's procedures:
- Qualification/validation plans (VP)
- Qualification protocols/reports (IQ, OQ, PQ, Hypercare)
Key skills and experience required include:
- Significant qualification experience in the pharmaceutical industry, ideally 5 years
- Good knowledge and significant experience in qualification
- CSV/data integrity (21 CFR part 11)
- Computerized/automated systems (SI/SA): Discoverant (Monitoring Process), Manufacturing Execution System (MES Batch record), Digital Plant Transformation (DPT)
- Equipment: Cap washing machine, autoclave, filling line, freeze dryer, sterilization tunnel, capping machine, data matrix engraving system, COP/SOP
- Fluent German (oral and written)
This is an excellent opportunity to work with a large pharmaceutical organization in Germany and contribute to the development of high-quality qualification documents.