For our client, a globally recognized leader in the development and manufacturing of high‑precision ophthalmic microsurgical instruments, we are looking for a motivated individual with initial experience in Quality Management within the Medical Device industry
Quality Engineer (a)
* Review and approve deviations, investigations and corrective and preventive actions (CAPAs) related to products and processes. Support during analysis, resolution and proper documentation of quality deviations
* Review and approve change documentation (CR). Organization of change control board
* Ensure compliance of production and development related documents with applicable regulations and standards such as EU-MDR, MDSAP and ISO 13485
* Analyze data trends to identify process improvement opportunities in collaboration with operational departments
* Support qualifications/validations and review validation documents
* First point of contact for quality and compliance related topics at the site
* Contribute to risk management as a core team member
* Contribute to local and international projects
* Degree in engineering or scientific discipline (university, HTL or equivalent)
* Industrial experience in the field of quality control / quality assurance / quality engineering
* Very good methodical analysis and problem solving skills
* GMP knowledge and practical experience
* Very good communication skills in German and English
Your application
Please apply online. For further information about the position, please contact your Gi Consultant, Mr. Nazim Sagkol (B. Eng.), (+41 76 349 85 07)
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