Supplier Quality Engineer

We are looking for an experienced Quality Engineer to lead supplier-side process validation and quality release activities for manufacturing transfers in a regulated environment. In this role, you will ensure production readiness by validating manufacturing processes, reviewing first-article inspections, and driving formal product release through established quality approval workflows.

You will work closely with engineering, supplier quality, and cross-functional teams to support successful product transfers while ensuring compliance with quality and regulatory standards.

• Lead supplier production line validation activities using the APQP framework.
• Execute and document process validation activities (IQ/OQ/PQ) to ensure manufacturing readiness.
• Conduct and review First Article Inspections (FAI), evaluating inspection data against product specifications and quality requirements.
• Perform final quality verification and authorize the formal release of products to manufacturing.
• Create, manage, and maintain validation and inspection documentation within SAP QMS and quality management systems.
• Route quality documentation through cross-functional approval workflows.
• Perform on-site inspections at the manufacturing facility when required and coordinate results with Supplier Quality teams.
• Partner with engineering, supplier quality, and program teams to resolve quality issues and support manufacturing transfers.
• Ensure compliance with applicable quality standards, procedures, and regulatory requirements.

• Bachelor's degree in Mechanical, Industrial, Biomedical, Electrical Engineering, or a related engineering discipline.
• 9–12 years of experience in Quality Engineering within the medical device or another highly regulated manufacturing environment.
• Strong knowledge of ISO 13485 quality management systems.
• Proven experience with APQP, PPAP, and process validation (IQ/OQ/PQ).
• Hands‑on ownership of First Article Inspection (FAI), including technical review and evaluation of inspection data.
• Experience working directly with manufacturing suppliers and driving quality approvals.
• Experience creating and managing quality documentation in SAP QMS or similar quality management systems.
• Excellent communication and cross‑functional collaboration skills.

• Experience with CPAP, ventilation, respiratory, or life‑support medical devices.
• Experience supporting manufacturing transfers or New Product Introduction (NPI) into production.
• Familiarity with supplier quality management and production readiness activities in regulated environments.

• An international community bringing together more than 110 different nationalities
• An environment where trust is central: 70% of our leaders started their careers at the entry level
• A strong training system with our internal Academy and more than 250 modules available
• A dynamic work environment that frequently comes together for internal events (after works, team buildings, etc.)

Amaris Consulting promotes equal opportunities. We are committed to bringing together people from diverse backgrounds and creating an inclusive work environment. In this regard, we welcome applications from all qualified individuals, regardless of sex, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.