Job Description
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)
Your tasks
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...
Quality Engineer (a)
Your tasks
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...
Apply for this Position
Ready to join Gi Group? Click the button below to submit your application.
Submit Application