• Support the design and testing of new products.

• Ensure that everything functions well and meets quality standards.

• Identify and prevent potential problems (especially risks, defects, and inspection issues).

• Ensure the product can be manufactured efficiently and safely.

• Support validations (process, tool, and equipment testing).

• Assist in the selection and approval of suppliers for new components or processes.

• Lead quality activities during design transfer (when the product moves from design to production).

• Work closely with engineering and manufacturing teams to ensure product quality and manufacturability.

Required:

• University degree in engineering (or similar).

• At least 2 years of experience in regulated industries, such as medical devices or pharmaceuticals.

• Understanding of manufacturing processes and quality tools such as FMEA (Failure Mode and Effects Analysis), CAPA (Corrective and Preventive Actions), PPAP (Production Part Approval Process), validations, and inspections.

• Knowledge of standards such as ISO 13485 (quality standard for medical devices).

• Advanced English communication skills (oral and written).

Desirable:

• Experience with Process Flow Mapping (PFM) or process risk assessment.

• Experience with non-conformity management.

• Experience with supplier quality initiatives.