Lead Qualification and Validation Engineer (m/f/d) - Visp
We are seeking a dedicated Lead Qualification and Validation Engineer to join our dynamic team in the pharmaceutical sector. This role is crucial for ensuring that all qualification and validation activities within pharma plants align with GMP regulations, thereby upholding product quality and compliance.
* Coordination of Activities: Spearhead the coordination efforts across various qualification and validation processes critical to pharmaceutical manufacturing environments.
* Risk Analysis: Conduct comprehensive risk analyses essential for maintaining process integrity and safety standards throughout production cycles.
* Broad Leadership Responsibilities: Potentially lead teams ranging from two to ten members, fostering an environment of collaboration while managing key project interfaces effectively.
Skill Requirements:
- Experienced in qualifications related or equivalent experience
- Familiarity with ISO13485/21 CFR Standards
This position requires substantial expertise within the realm of Pharmaceutical Manufacturing, promising professional growth through challenging yet rewarding tasks. Join us at this pivotal moment as we advance health solutions globally by applying today!
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