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Automation Systems Validation Expert
3 weeks ago
We are seeking an Automation Specialist to join our team. The ideal candidate will have hands-on experience in equipment qualification and computerized system validation.
About the RoleThis is a mid-senior level full-time position that involves driving qualification and validation activities for automation and computerized systems.
The successful candidate will be responsible for reviewing and approving URS, DQ, IQ, OQ, PQ documentation.
- Drive qualification and validation activities for automation and computerized systems.
- Review and approve URS, DQ, IQ, OQ, PQ documentation.
- Ensure cGMP compliance across all validation phases.
To be considered for this role, you will need:
- A degree in Engineering or a Scientific discipline.
- 3+ years of hands-on experience in equipment qualification and computerized system validation in the pharmaceutical industry.
- Strong knowledge of GxP, GAMP, ISPE guidelines, and regulatory expectations.
- Excellent communication and documentation skills.
This is a great opportunity to work with a leading global pharmaceutical CDMO. You will have the chance to collaborate with QA, Engineering, and IT teams to ensure systems are validated and compliant throughout their lifecycle.
Location: EU-based site (Relocation support available for the right candidate).
