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 t...