Software QA Engineer 1
FULL TIME
mid
Salary
No salary data
vs. Engineering avg
Ghost Score
Worse than category average
Engineering jobs
Freshness
Posted 1 months ago
Required Skills
Job Description
Dexcom Corporation is a pioneer and global leader in continuous glucose monitoring (CGM). They are seeking a Software QA Engineer 1 to provide technical support and guidance to software teams, ensuring compliance with software development processes and quality standards while focusing on product improvement and defect prevention.
Responsibilities:
Actively participates as a core team member of the R&D Quality Assurance Engineering team; Strong understanding of, and ability to provide guidance on IEC 62304, 21 CFR 820, and other relevant regulations worldwide; Lead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation across software teams, including:; Drive Pre-market risk management deliverables like SHA, design FMEA and support Cyber security risk management; Provide guidance to Software Design and test teams, support Software configuration management, tool validations and software integrations; Reviews and approves all software design control deliverables; Support post market activities related to Software anomalies, risk assessments and CAPA activities (if applicable); Lead and support R&D SW Design Assurance efforts including continuous improvement opportunities for products and processes; Responsible for reviewing, authoring, and revising appropriate technical documentation including design history files, standard operating procedures, protocols, reports, etc; Assesses the impact of change control to ensure no adverse impact on product performance and a state of compliance is maintained; Effectively communicates with the broad Dexcom team and upper-level management on plans, status of tasks, project progress and challenges; Assumes and performs other duties as assigned
Qualifications:
Strong understanding of, and ability to provide guidance on IEC 62304, 21 CFR 820, and other relevant regulations worldwide; Medical Device experience in compliance with the requirements of FDA 21 CFR Part 820, IEC 62304, ISO 13485; Knowledge and experience with SDLC processes along with software development methodologies such as Agile Software Development, Waterfall Model, etc; Software Quality or Engineering experience in Requirements Analysis, Design/Development, Product Integration and Test; Ability to interpret software design and code to verify implementation of requirements; Software development and/or Software test experience; Ability to communicate and present to all levels of management; Ability to understand complex tasks and goals. Drive projects to completion with limited supervision; Experience working with cloud-based systems; Typically requires a bachelor's degree in a technical discipline, and a minimum of 0-2 years of related experience
Required Skills:
IEC 62304, 21 CFR 820, ISO 13485, Software Development Life Cycle (SDLC), Agile Software Development, Waterfall Model, Requirements Analysis, Software Quality, Software Development, Software Testing, Cloud-based Systems, Cyber Security, Communication, Problem solving, Adaptability
Ghost Score Breakdown
Posted 30-59 days ago
+ ptsNo salary info
+ ptsNo company logo
+ ptsKnown scam/ghost company
Reposted listing
Expired deadline
High job-to-employee ratio
Recruiting agency
Overall: 34/100Moderate Ghost Risk
Application Tips
- Top skills mentioned: r, agile, monitoring. Make sure your resume highlights these.
- This listing has some uncertain signals. Research the company before applying.