CH - Senior Engineer für Qualifizierung und Validierung (m/w/d) - 100%

Possible work locations

Visp

Type of employment

Full-time

As part of our team, you will be responsible for qualification and validation activities of pharmaceutical process systems in compliance with current GMP regulations. You will work on exciting and attractive projects and support the growth of our company in close collaboration with team leadership.

Your contribution to our success:

• Coordination and execution of project-specific qualification and validation activities in accordance with current GMP regulations
• Development and implementation of qualification and validation systems
• Support in the preparation of overarching qualification and validation documentation
• Conducting and moderating risk analyses
• Project acquisition and client support
• Supporting team leadership in process development and employee mentoring
• Close collaboration with current team leadership and gradua...