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Equipment Qualification Specialist F/M
Il y a 3 mois
Are you seeking a rewarding position within the pharmaceutical sector? We are currently looking for a Specialist in Equipment Qualification and Validation F/M.
Key Responsibilities:
- Oversee the qualification and validation processes for equipment in accordance with the established master plan.
- Act as the project manager for validation initiatives: Evaluate supplier documentation, Create and review exercise protocols and reports (IQ, OQ, PQ), Develop testing protocols (QI, QO, FAT, SAT), Conduct or assess equipment testing, Generate reports for any anomalies or deviations identified during testing.
Qualifications:
- Degree in engineering or a related field (Bac + 5).
- Demonstrated experience in equipment qualification and validation within the pharmaceutical industry.
- Familiarity with applicable standards (GMP, Part 11 requirements).
- Fluent in professional English.
- Proactive, detail-oriented, and responsive.
- Knowledge of HSE regulations is advantageous.
At CONSULTYS, we are dedicated to fostering a culture of innovation and excellence. We prioritize diversity and inclusion, ensuring support for individuals with disabilities.
