Sr Quality Engineer

• 3–7 years experience as a quality engineer in the medical device industry
• Hands-on manufacturing quality — incoming inspection, FAI, final product release
• Engineering drawing interpretation and GD&T
• CAPA management from initiation through to closure and verification of effectiveness
• Nonconformance documentation and follow-up
• Supplier quality management including ASL maintenance and SCAR programme
• Working knowledge of FDA QSR / 21 CFR 820 and ISO 13485

The following skills would also be beneficial

• Design control experience — document reviews, design outputs, DHF and DMR maintenance
• V&V protocol and report writing
• ASQ CQE certification
• Experience supporting internal and external audits

You must be comfortable working independently and taking ownership of quality processes without significant hand-holding, while also being a collaborative member of a small engineering team. This is a hands-on, build-it-from-the-ground-up role in a startup environment — the kind of position that suits someone who enjoys variety and accountability in equal measure.

You will be joining a pioneering surgical robotics company developing AI-driven, imaging-guided robotic systems for ophthalmic surgery — technology that directly improves patient outcomes and expands access to high-quality surgical care.