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
+ pts
No salary info
+ pts
No company logo
+ pts
Known 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.

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