Supplier Quality Engineer

Are you an experienced Quality, Supplier, or Process Validation Engineer looking to make a meaningful impact in the medical device industry?

Would you like to shape the future of life-saving implantable technologies in a collaborative and fast-paced environment?

Join our client’s growing Operations and Quality team and play a critical role in ensuring robust processes and high-quality outcomes across internal and external manufacturing.

Key Responsibilities :

• Lead the planning and execution of process validations (IQ, OQ, PQ) for both internal and supplier-based manufacturing processes.
• Develop efficient, risk-based validation strategies that balance quality, compliance, and business timelines.
• Support and challenge external supplier validations and ensure alignment with internal standards and regulatory expectations.
• Maintain and improve the Quality Management System in line with ISO 13485 and FDA regulations.
• Lead or contribute to supplier development activities during the design transfer phase, ensuring suppliers meet quality, technical, and timeline requirements.
• Drive continuous improvement in supplier quality, process capability, and risk mitigation.
• Collaborate cross-functionally with R&D, Regulatory Affairs, and Manufacturing to support product industrialization.
• Serve as a project lead on validation and supplier-related initiatives, managing external partners with appropriate oversight and escalation.

Requirements :

• Degree in Engineering, Life Sciences, or a related technical field.
• Several years of experience in the medical device industry, ideally in Supplier Engineering, Process Validation, Quality Engineering, or Project Management roles.
• Deep understanding of quality management systems (QMS) and regulatory requirements (ISO 13485, FDA 21 CFR Part 820).
• Strong knowledge of manufacturing processes (e.g., injection moulding, machining, extrusion) and validation principles.
• Proven ability to lead projects and work effectively with external partners and suppliers.
• Risk-based mindset with excellent documentation and analytical skills.
• Strong communication skills in English; German is a plus.

What’s in it for you?

• Join a purpose-driven company focused on breakthrough implantable devices.
• Work in a cross-functional, international environment where your input directly impacts patient lives.
• Enjoy diverse challenges across quality, operations, and supplier development.
• Be part of a high-growth organization with opportunities for personal and professional development.

If you’re passionate about ensuring quality and process excellence in the medical device space, apply now and / or contact Hollie Dear at Adaptive Life Science for more information!

Supplier Quality Engineer • Munich, Bavaria, Germany