Quality System Manager / Lead Auditor

What we have to offer You can expect a challenging and rewarding role with real impact, where you can actively shape structures and processes. You will work in a professional, collaborative environment that values initiative, responsibility, and continuous development. Interested? For further information, Sarah Calvi and Barbara Tomljenovic will be happy to assist you at . Please submit your complete application documents via application button.

• University degree in life sciences, engineering, or a related field (or equivalent qualification)
• 3+ years of applied quality management experience in life sciences or another regulated industry (ideally dental/medical devices) with strong ISO 13485 know-how Education in regulations such as European Medical Device Regulations, Swiss Medical Device Ordinance, US 21 CFR and the ability to translate requirements into practical QMS solutions, completion of ISO 13485 and ISO 19011 training course, incl. certification
• 3+ years of professional experience in audit planning and execution
• Excellent communication and strong stakeholder management skills, ability to build strong relationships and act as team player
• Strong result orientation and business sense
• Well-organized and structured, self-starting, and comfortable working independently in a fast-paced, international environment.
• Languages: English fluent; German fluent; additional languages welcome