
QA engineer
Job description
About the Position
A startup company in the field of medical devices is looking for a skilled and energetic QA engineer with a “hands-on” and “can-do” approach who wants to join our fast-growing company. The QA engineer is the team’s technical and functional authority in testing and verifying our new visionary technology. S/he will work with the R&D team and report to the CTO.
Responsibilities
- Design, write, and maintain testing documentation and protocols for complex embedded systems in accordance with medical device standards and selected regulations.
- Analyze functional and technical documents (product requirement, certification, etc.)
- Execute functional software and hardware testing in-house and at customer sites including, product test plan, test case scenarios, and reports.
- Plan and build testing environment and tools that comply with requirements, intended use, and regulatory guidelines.
- Support lab testing and certification process of hardware.
- Be up to date with medical regulation and guidelines related to company product testing.
- Ensure that the progress is according to the quality requirements.
- Oversee and maintain testing log files, severity, and triage of bugs and defects.
- Where applicable, support field testing, customer support, and MRB activities.
Requirements
- 2+ years of QA experience testing WEB & Mobile Applications.
- Experience with end-to-end testing of embedded medical device systems coupled with digital health.
- Experience in testing both Client & Server sides.
- Experience with writing STP, STD, and protocols.
- Experience with system certification process - a plus.
- Experience with in-vitro and clinical testing - a plus.
- Experience with medical device standards - a plus.
- Experience in a fast-paced, start-up like environment - a plus.
Qualifications
- Well organized and methodological attitude.
- Creative and thoughtful “hands-on” leader with a “can-do” approach.
- Self-motivated, ability to work autonomously in a small team environment.
- Out of the box and a “big-picture” thinker.
- Ability to focus on deadlines and deliverables.
- Ability to drill down and find the root cause of problems.
- Excellent verbal and written communication skills (Fluent English).
- Must be comfortable working in an environment controlled by standards and regulations, such as Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and Quality System Regulations (QSRs), both US and international.
- Ability/willingness to travel internationally, up to 20%.
We Offer
- Opportunity to work in a fast-growing startup in the medical devices field.
- Collaborative and innovative work environment.
- Professional growth and development opportunities.
About the Company
Our company is a startup in the field of medical devices, dedicated to developing visionary technology and products. We are committed to quality and innovation, and we are looking for passionate and skilled individuals to join our team.
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