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.

Explore Your Tasks And Responsibilities

• 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

Show Your Expertise

• 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)

Contact You want to be part of the Exyte team? We look forward to receiving your application!

For further questions and information, please do not hesitate to contact Ilayda Öztürk via E-Mail at [email protected].

Please note that we only consider applications submitted through our application portal. Applications sent via email will not be considered due to data protection regulations.