Job Opportunities API

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.