Opportunity to join a global medical device manufacturer as Quality Engineering Manager.You'll be responsible for overseeing a small team of quaility & validation engineers through manufacturing, labelling & packaging change initiatives.
Responsibilities
- Manage the quality engineering processes, including risk management, design control, process validation, and change control.
- Ensure compliance with FDA regulations, ISO standards, and other relevant regulatory requirements.
- Collaborate with cross-functional teams including R&D, manufacturing, and regulatory affairs to establish and maintain quality standards.
Experience Required
- 6 years' Quality Engineering experience with knowledge of the Medical Devices and FDA, ISO:13485.
- 3 years' management experience, performing day-to-day management responsibilities and perfromance reviews.