Senior Engineer CQV; m​/f​/d

Discover your exciting role

Shape innovative projects in the pharmaceutical industry and take on responsibility in exciting qualification and validation projects within a dynamic environment at Exyte.

• Preparation of qualification and validation plans
• Preparation and review of specifications, risk analyses, design documents, and project processes
• Planning and execution of DQ, IQ, OQ, and PQ for production equipment
• Preparation of qualification reports
• Review of supplier documentation and coordination of supplier activities
• GMP-compliant documentation of executed work
• Handling of changes and deviations (Change Control & Deviations)
• Preparation of Standard Operating Procedures (SOPs)
• Maintenance and archiving of documentation
• Ensuring training standards of project team members
• Leading a project team (up to 3 people)
• Project management of smaller projects (time, budget, resources)
• Supporting and mentoring junior engineers
• Independent execution of work packages (WPs) and smaller projects

• Degree in engineering, natural sciences, or a pharmaceutical-related field
• Willingness to travel within Switzerland
• Strong knowledge of GMP regulations and common industry standards
• High level of quality awareness and attention to detail in documentation
• Several years of professional experience in the pharmaceutical industry
• Very good German and good English skills (corporate language)