Supplier Quality Engineer (m/f)

Bachelor’s degree in Engineering, Quality, Life Sciences, or related field., 3–7+ years of work experience in supplier quality, quality engineering, or manufacturing quality in medical devices, pharmaceuticals, or regulated packaging., Strong knowledge of ISO 13485, GMP, FDA regulations, and/or EU MDR., Experience with supplier audits, CAPA, root cause analysis, and risk management tools., Familiarity with packaging materials (plastics, sterile barriers, labels, cartons) and validation requirements is highly desirable., Ability to interpret technical drawings, specifications, and validation protocols., Willing to learn, independent, initiative and proactive, Self-motivated and able to work in a team and with minimum supervision, Strong project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner., Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing)., Fluent in English, both written and spoken

myBenefit, sharing the costs of sports activities, private medical care, fruits, integration events, dental care, corporate gym, mobile phone available for private use, coffee / tea, drinks, parking space for employees, leisure zone, extra social benefits, pre-paid cards, holiday funds, baby layette, christmas gifts, opportunity to obtain permits and licenses, charity initiatives