Senior QA Validation Engineer

SoCode

Town of Cambridge

Hybrid

AUD 153,000 - 192,000

Full time

2 days ago
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Benefits offered by this job

Bonus
Equity

Job summary

SoCode in Cambridge seeks a Senior QA Validation Engineer to lead verification and validation of safety-critical software within a regulated environment, ensuring compliance with quality management standards. You will shape test strategy, develop automated tests, and drive efficient execution across the full software lifecycle.

Collaborating with software, systems, quality, and regulatory teams, you will document results, support audits, and contribute to risk management and continuous process

Qualifications

  • Bachelor's or Master's in Engineering, Computer Science, or related field.
  • Several years of software QA in a regulated environment.
  • Experience with automated and manual test strategies.
  • Familiarity with C/C++ and Python for test development.
  • Knowledge of electronic quality management systems (eQMS) and controlled docs.
  • Ability to analyze issues, assess risks, and propose practical solutions.
  • Excellent communication and stakeholder management.

Responsibilities

  • Develop and maintain verification and validation plans, protocols, and reports.
  • Define test strategies for unit, integration, system, and end-to-end testing.
  • Design and maintain automated test frameworks and suites.
  • Support regulatory compliance activities and documentation.
  • Collaborate with software, quality, regulatory teams to improve processes.
  • Assist in audits and inspections as required.

Skills

Software verification
Software validation
Quality assurance
Automated testing
Manual testing
Regulated environment
C/C++
Python
Stakeholder management

Education

Engineering degree
Computer Science
Biomedical Engineering

Tools

eQMS
Test automation frameworks

Job description

Posted 20 October 2026 Salary £80000 - £100000 per annum, Benefits: Bonus Location Cambridge Job type Permanent Discipline Software Testing and Quality Assurance Reference AB-83

Job Title: Senior QA Validation Engineer

Location - Cambridge: On Site (some flex on occasion)

Salary

-£80k - £100k (depending on experience) + up to 10% bonus (company performance dependent) + equity

Overview

We are seeking an experienced Senior QA Validation Engineer to support the development and delivery of complex, safety-critical software systems within a regulated environment. This role combines software verification and validation activities with quality and compliance responsibilities, ensuring that software products are developed, tested, and documented in accordance with established quality management processes and industry standards. Working closely with cross-functional engineering teams, you will contribute throughout the software development lifecycle, from test strategy and verification planning through to execution, reporting, and regulatory compliance activities.

Key Responsibilities
Verification & Validation
  • Develop, maintain, and execute software verification and validation plans, protocols, and reports.
  • Define and implement test strategies covering unit, integration, system, and end-to-end testing activities.
  • Design, develop, and maintain automated test frameworks and test suites to support continuous integration and release activities.
  • Create and maintain test tools and processes to improve test coverage, efficiency, and repeatability.
  • Execute manual testing where automation is not feasible or appropriate.
  • Establish and maintain traceability between requirements, design artefacts, risk controls, and verification activities.
  • Analyse test results, investigate defects, and support root cause analysis and corrective actions.
Quality & Compliance
  • Ensure testing activities are conducted in accordance with established quality management processes and applicable regulatory requirements.
  • Support software risk management activities throughout the product lifecycle.
  • Author, review, and maintain validation documentation, including test plans, test cases, protocols, reports, and supporting quality records.
  • Contribute to design history, requirements management, and other controlled documentation activities.
  • Support internal and external audits, inspections, and regulatory submissions where required.
Collaboration
  • Work closely with software, systems, quality, and regulatory teams to ensure product quality objectives are achieved.
  • Collaborate with stakeholders across engineering and operations to resolve quality issues and improve development processes.
  • Promote best practices in software testing, validation, and quality assurance.
Skills & Experience
  • Strong background in software verification, validation, and quality assurance within a regulated industry.
  • Experience developing and executing automated and manual test strategies.
  • Working knowledge of C/C++ and Python for test development and automation.
  • Experience testing complex integrated systems involving software, hardware, and electromechanical components.
  • Familiarity with requirements management, electronic quality management systems (eQMS), and controlled documentation processes.
  • Ability to analyse technical issues, identify risks, and develop practical solutions.
  • Excellent communication and stakeholder management skills.
Preferred Experience
  • Experience working within regulated product development environments.
  • Knowledge of software lifecycle, risk management, and quality management standards relevant to safety-critical systems.
  • Experience supporting compliance, validation, and regulatory documentation activities.
    Qualifications
    • Bachelor's or Master's degree in Engineering, Computer Science, Biomedical Engineering, or a related technical discipline.
    • Several years of experience in software quality assurance, verification, validation, or test engineering within a regulated industry.
    Working Environment
    • Collaborative, fast-paced engineering environment.
    • Opportunity to work across software quality, validation, compliance, and process improvement activities.
    • Occasional travel may be required.
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