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/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 CF 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!
