Senior Software Coe Manager

Philips UK

**
8+ years software engineering in medical devices
Software requirement and system design expertise
Regulatory compliance and cybersecurity management
** Philips UK is seeking a Senior Software CoE Manager to lead their Software Center of Excellence team within the CT Software Organization. The role emphasizes driving engineering excellence, regulatory compliance, and innovation in software development, particularly in the medical devices sector. **

Job Summary

  • The role leads the Software Center of Excellence to drive engineering excellence by governing requirements, system design, and regulatory compliance within the CT Software Organization.
  • Candidates must oversee cybersecurity as Security Owner, manage vulnerability scanning, and integrate DFMEA into early design phases to mitigate risks effectively.
  • The position champions innovation by pioneering Spec-Driven Development and orchestrating AI Agent workflows to automatically generate code and tests from structured specifications.

Matching Summary

Match Score: 75

** Philips UK is seeking a Senior Software CoE Manager to lead their Software Center of Excellence team within the CT Software Organization. The role emphasizes driving engineering excellence, regulatory compliance, and innovation in software development, particularly in the medical devices sector. **

Skills & Requirements

Must-have

  • 8+ years software engineering in medical devices
  • Software Requirement and System Design expertise
  • Regulatory compliance and cybersecurity management
  • DFMEA and risk control implementation
  • Security Owner responsibilities for CT Software
  • Spec-Driven Development (SDD) methodologies

Nice-to-have

  • Experience with AI Agent-assisted workflows
  • Prompt Engineering skills
  • Agile and DevOps transformation leadership
  • Strategic planning and business acumen
  • Mentoring and talent development focus

Key Requirements

  • Bachelor's or Master's degree in Computer Science or related field
  • Minimum 8+ years experience in Medical Devices or safety-critical industries
  • Proven track record translating clinical needs into technical specifications

Work Rights

Not specified

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