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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 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.