QA Engineer
Augmedics
Software Engineering, Quality Assurance
Israel
Posted on Jan 24, 2025
Description
Augmedics, a medical device start-up developing an Augmented Reality Guided Surgery System, is seeking for a QA Engineer.
The QA Engineer at Augmedics is responsible for developing and maintaining the company’s Quality Management System in accordance with various medical device requirements.
We are located in Yokneam.
Main responsibilities:
- Work closely with the engineering, operations and supply chain teams, both in Israel and the USA, providing ongoing (sustain) product support and supporting NPI activities (e.g., parts and materials specifications, equipment qualification, facility and infrastructure qualification and process controls.
- Good mechanical and electrical knowledge to enable conducting process nonconformities investigations and implementation of corrective actions.
- Leading and supporting CAPA activities.
- Supplier Quality: Approval of new suppliers, analyse supplier’s performance, Supplier auditing and SCAR management.
- Proactively initiate and support process improvements, through improved process controls, statistical techniques and use of various production related SW tools.
- Supporting Computer Software Validation activities both in R&D and production, Understanding 21CFR part11 requirements.
- Auditing: Perform internal auditing in accordance with ISO19011 and support all activities related to external audits.
Requirements
- BSc degree in Engineering or relevant field – A must.
- CQE / CMQ certification – An advantage.
- Minimum 3 years experience as a QA Engineer in a medical device company - A must
- A good knowledge of Medical Device Manufacturers requirements (e.g. FDA GMP per 21CFR Part 820, ISO:13485, MDSAP, and others).
- Certified internal auditor – A must,
- A lead auditor certification – An advantage.
- In-depth understanding of technical documentation and problem-solving abilities.
- Familiarity with statistical analysis.
- Knowledge in the requirements for ISMS per ISO27001:2022 – An advantage.
- Proven experience in leading and managing Corrective & preventive action implementation in a multi-disciplinary medical device.
- Highly motivated and self-driven person capable of adjusting quickly to changes, Great attention to details.
- Fluent English.