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Validation Engineer for Pharmaceutical Equipment
Il y a 3 mois
Exciting Career Opportunity:
We are seeking a Validation Equipment Specialist to become a vital part of our team within the pharmaceutical sector. Your primary responsibilities will encompass:
- Overseeing qualification and validation processes for equipment and methodologies,
- Evaluating protocols and documentation provided by vendors,
- Creating protocols and reports for validation activities (IQ, OQ, PQ),
- Drafting testing protocols (QI, QO, FAT, SAT),
- Conducting or assessing equipment testing procedures,
- Recording any anomalies or deviations encountered during validation activities.
About You:
- Possess an engineering degree (Bachelor's + 5 years of experience),
- Have 3 to 5 years of experience in equipment qualification and validation within the pharmaceutical field,
- Be knowledgeable about applicable standards (GMP, Part 11 requirements),
- Exhibit proficiency in professional English,
- Demonstrate a dynamic, responsive, and detail-oriented approach,
- Understanding of HSE regulations is advantageous.
Why Join Our Team:
Are you interested in being part of a small-sized organization that emphasizes individual development and performance?
Do you want to engage in innovative projects with a long-term vision?
Would you like to contribute your expertise in a collaborative team setting?
If this resonates with you, Join Us at CONSULTYS, where we prioritize diversity and inclusion, and support individuals with disabilities.
