Be the Candidate They Can't Ignore.

Don't just send a resume; set yourself up so the right work finds you.

  • Look like a pro instantly with a stunning personal brand.

  • Gain instant "Top Ten" status so you aren't just another name in a pile.

  • Wake up to booked meetings instead of "rejection" emails.

Join the Club — Free Forever

Software Quality Assurance (SQA) Engineer (part-time) IRC302996

  • Source: LinkedIn
  • GlobalLogic
  • On-site
  • Lviv
  • Mid level

Job Description

Description The client is a global leader in the medical technology sector, specializing in advanced diagnostic and surgical systems that combine precision mechanics, real-time control, and highfidelity imaging.

GlobalLogic is driving the engineering, quality, and regulatory alignment for next-generation MedTech solutions, medical cloud platforms, and connected clinical diagnostic technologies. The platform integrates cloud-native microservices (.NET / Java), enterprise databases, embedded software components, and real-time clinical workflows operating under strict international medical device standards and cybersecurity frameworks.

The Senior Software Quality Engineer (SQA) will drive, execute, and maintain the Software Quality Assurance strategy across the entire software development life cycle (SDLC). Operating within an Agile/hybrid delivery model, the engineer ensures that all engineering processes, risk management activities, automated quality gates, and software deliverables comply with Client’s Quality Management System (QMS)and regulatory requirements.

Requirements

  • Bachelor’s degree or higher in Software Engineering, Biomedical Engineering, Electrical Engineering, Computer Science, or a related technical discipline.
  • 5+ years of experience in Software Quality Assurance or Quality Engineering within the medical device industry, specifically working with Software as a Medical Device (SaMD) or complex embedded/cloud medical systems.
  • Proven track record of executing SQA strategies, defining quality metrics, mentoring peer engineers, and driving QMS process adoption within cross-functional delivery teams.
  • Practical understanding of core medical device standards and regulations: ISO 13485, IEC 62304, ISO 14971, and FDA Quality System Regulation (21 CFR Part 820).
  • Hands-on expertise in authoring and executing complex Software V&V strategies, preparing Design History Files (DHF), maintaining Traceability Matrices (RTM), and evaluating test evidence across manual and automated testing streams.
  • Experience in risk analysis methodologies (FMEA, FTA, Hazard Analysis), non-conformance triage, CAPA investigations, and defect root-cause resolution.
  • Strong familiarity with software development concepts like: cloud infrastructure (Azure/AWS), programming languages (.NET, Java, C++), API architectures.
  • Practical experience integrating QMS quality gates with modern CI/CD pipelines, static analysis scanning (SAST/SCA), and automated testing frameworks (AQA).
  • Participating in internal QMS audits and serving as a technical SQA subject matter expert during external regulatory inspections (FDA, Notified Bodies).

Job responsibilities

  • Implement and maintain project-specific Software Quality Assurance plans aligned with Hologic’s QMS; ensure IEC 62304-compliant Agile/hybrid SDLC workflows and track quality KPIs (e.g., test coverage, defect leakage, audit readiness).
  • Review and author critical software lifecycle deliverables, including Software Development Plans, SRS, Architecture & Design Specifications, Risk Management Files, V&V Plans/Reports, and Usability Engineering files (IEC 62366).
  • Support software risk management activities, ensuring software hazards are properly identified, risks are assessed, and control measures are accurately implemented and verified.
  • Drive the software V&V process, ensuring testing strategies (both manual and automated) provide comprehensive coverage based on requirements and identified risks.
  • Participate in internal quality audits of software processes and technical documentation; serve as an SQA technical representative during external client audits, FDA inspections, and Notified Body reviews.
  • Enforce Definition of Done (DoD) blocking rules in CI/CD pipelines, execute software change control procedures, and triage software defects to prevent non-conformances from reaching release stages.
  • Guide developers, architects, and QA engineers on QMS procedures, regulatory standards, and software quality best practices to foster engineering excellence and patient safety.
  • Deliver release readiness assessments, compliance summaries, and defect metric trends to Delivery Managers, Solution Architects, Lead SQA Engineers, and Hologic quality leadership.

What we offer

Empowering Projects: With 500+ clients spanning diverse industries and domains, we provide an exciting opportunity to contribute to groundbreaking projects that leverage …

Skills

  • microsoft-azure
  • amazon-web-services
  • Java
  • cplusplus

Create Free Account & Apply
  • Free personal website
  • Built-in Talent Agent
  • Apply to future jobs in 1 click
  • Get matched to similar roles
or
Apply as a guest this time

You'll apply successfully, but won't be able to track your application, save this job, or get matched to similar roles.

This listing is a publicly available opportunity curated by Try Club to help talent discover relevant roles. Try Club is an independent platform and is not affiliated with GlobalLogic

Get Similar Jobs

Browse more similar roles on TRY and find your perfect match.

Show Me Similar Jobs

Stop Searching. Start Thriving.

Why waste time chasing leads when the perfect projects can find you?
With TRY, clients actively searching for professionals with your skills can discover you in seconds. Whether it's a quick gig or your dream role, we connect you with opportunities that matter.

  • Get found faster
  • Let projects come to you
  • Build a career on your terms

Take control of your career today.

Claim Free Website in 2 Minutes