صاحب العمل نشط
- Own the companys Software Quality Assurance process including the software validation testing activity and associated documentation
- Review and approve software product documentation (SRS, SDS)
- Create and execute test cases to ensure the quality of our software products
- Log and verify bugs and aid in associated root cause investigation and corrective action activity
- Work closely with our development team to ensure the timely delivery of high-quality software products
- Conduct performance, load, and stress testing and continuously break and test things to achieve to identify and resolve potential performance issues
- Work closely with our design team to ensure that software products are in line with the desired specifications and user requirements
- Develop and maintain testing documentation, including test plans, test cases, and test reports
- At least 5 years of experience in software quality assurance for Class II and III medical devices
- Software validation experience for a regulatory submission and completion of New Product Development (NPD) for a Class II and/or Class III medical device
- Working knowledge of current regulatory industry standard requirements such as FDA 21 CFR Part 11& Part 820, ISO 13485:2016, and IEC 62304:2006 is required
- Can own the QA process from start to finish
- Linux experience is a plus
- Bachelors degree in Computer Science, Engineering, or a related field
- Fully vaccinated against COVID-19
- Competitive salary and benefits package
- Hybrid work set-up
- Your work will have an immediate impact on our products
- You have the autonomy to decide your terms
- Career growth
- Youll get to enjoy all the benefits that come from being part of a small, growing, well-funded company
دوام كامل