
Quality Assurance Medical Devices
- Göteborg
- Tillfälligt
- Heltid
- Identify, define, and implement improvement opportunities within QMS processes
- Review and approve quality procedures in line with ISO, MDSAP, and MDR 2017/745 requirements.
- Lead and drive investigations related to non-conformities (NCs) and Corrective and Preventive Actions (CAPAs).
- Review Change Requests (CR) and Change Order checklists concerning QA.
- Collaborate with cross-functional teams to approve temporary non-conformities.
- Hybrid setup possible, with at least 60% onsite presence required.
- Start date: ASAP.
- Strong experience in Quality Assurance, Test, and Validation within medical devices.
- Proven knowledge of applicable regulatory frameworks (ISO, MDSAP, MDR 2017/745).
- Ability to collaborate effectively across different functions and drive QA initiatives.
- Secure & Transparent Employment We follow the Teknikföretagen (Almega) collective agreement, ensuring fair compensation, benefits, and long-term stability.
- Diverse Industry Exposure Work on high-impact projects across Telecom, Automotive, Retail, and Banking, gaining experience that spans multiple sectors.
- Accelerated Career Growth Whether you're a seasoned developer or an emerging tech leader, we offer continuous learning, challenging assignments, and leadership opportunities to help you grow fast and grow smart.
- Culture of Collaboration & Curiosity Join a team that values innovation, inclusion, and integrity. At VIPAS, your ideas matter, your voice is heard, and your growth is celebrated.