paycor
Associate Software V&V Engineer
Sciton
Palo Alto, USA
Full-time
No Prior Experience Required
Onsite
USD 70000-80000 yearly
Discovered 1 weeks ago
Free
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- Develop, extend, and execute test plans and protocols for Sciton’s medical devices, and write reports.
- Identify and correct defects with the software team.
- Perform risk analysis on software requirements and changes.
- Communicate significant issues and recommend process improvements.
- BS in Software Engineering, Computer Science, or a related field.
- 0–2 years of experience in software quality assurance, software validation, or a related role, preferably in an FDA-regulated environment.
- Basic understanding of software validation and software development life cycle requirements in regulated environments.
- Strong technical writing, interpersonal communication, critical thinking, problem-solving, and collaborative skills.
- Familiarity with product development and lifecycle processes for medical devices, including 510(k) and/or ISO-regulated product development.
- Familiarity with IEC 62304 and software lifecycle processes for medical devices.
About Sciton
Medical Device Manufacturing512 employeesFounded 1997
Employee-owned medical device manufacturer producing aesthetic and medical lasers and light systems for medical professionals.
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