Quality Assurance Engineer

About the role

The Quality Assurance Engineer will ensure that Corin’s products, procedures and policies meet the highest quality standards. This role supports both incoming goods inspection and final product release within a regulated medical‑device environment.

Key responsibilities

• Control quality of production processes and conduct incoming inspections.
• Maintain the quality and documentation management system.
• Provide quality input to CAPA investigations, non‑conformances, concessions, deviations and change control.
• Offer technical guidance to Production Engineering, Quality, marketing and R&D teams.
• Monitor and report on quality and production processes.
• Contribute to quality management system procedures.
• Conduct internal audits in accordance with ISO 13485 and 21 CFR 820.
• Support supplier evaluation and approval.
• Ensure process validation complies with applicable medical‑device standards.

Required profile

• Bachelor’s degree in Life Sciences, Medical or Engineering.
• 2‑5 years experience in a medical‑device or pharmaceutical organization.
• Engineering background (Mechatronics, Electrical, Biomedical, Mechanical, Software or Computer Science) is advantageous.
• Ability to work autonomously and within a team.
• Knowledge of regulatory and quality system requirements.
• Experience in regulated product development and generation of V&V, test plans and procedures.

Required skills

• ISO 13485
• 21 CFR 820
• V&V planning

What we offer

• Wellbeing subsidy
• Birthday leave
• Supportive culture
• Ongoing training programs
• Equal employment opportunity