Job Description
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...
Apply for This Position
Ready to take the next step? Click the button below to submit your application.
Submit Application