Qualitätsmanager (m/w/d)

This position involves supporting the Quality Manager with daily operations and co-developing the company’s quality management system for European and US markets. The role includes conducting internal audits and assisting with external inspections by authorities and notified bodies. You will coordinate corrective and preventive action processes while ensuring product safety globally. Additionally, you will provide quality-related support to production, research and development, and regulatory affairs teams. The employer requires a university degree in medical technology, regulatory affairs, or a comparable field. Candidates must have at least three years of professional experience in quality management within a medical device manufacturer. Specific knowledge of standards such as FDA regulations, MDR, and ISO 13485 is essential. Familiarity with various sterilization methods is considered a plus but is not mandatory. The text does not specify language requirements, working arrangements, or shift patterns. This opportunity suits professionals who want to contribute to a young, award-winning MedTech company focused on innovative wound healing solutions.