As Product Quality Manager, you will be responsible for ensuring product quality, regulatory compliance, and patient safety across the full product lifecycle — from design and development through supplier management and distribution. You will play a key role in maintaining ISO 13485 compliance and supporting MDR requirements while collaborating closely with cross-functional stakeholders including Regulatory Affairs, R&D, Operations, Supply Chain, and external suppliers. Key Responsibilities

• Ensure product compliance with ISO 13485 and MDR
• Oversee supplier quality management, audits, CAPA, and SCAR processes
• Support design quality, risk management, and design transfer activities
• Provide quality input during product development and lifecycle management
• Monitor product verification and validation activities
• Safeguard quality within logistics and distribution processes
• Maintain and improve QMS processes
• Support internal and external audits

Your Profile

• Bachelor’s degree in Engineering, Quality Management, or related field
• Strong experience in Medical Device Quality Management
• Solid knowledge of ISO 13485 and MDR
• Experience with supplier audits and quality oversight
• Background in design quality or new product introduction
• Strong analytical and communication skills
• Fluent in English

Offer

• Competitive base salary with annual bonus
• Premium-free pension scheme
• 30 days annual leave
• Hybrid working model
• Collective health insurance discounts
• Employee discounts on selected products
• International, purpose-driven work environment with growth opportunities