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Global Head Commissioning, Qualification & Validation (CQV)

GE Healthcare

Engineering Jobs

Global Head Commissioning, Qualification & Validation (CQV)

full-timePosted: Jan 14, 2026

Job Description

Job Description Summary

As the Global Head of Commissioning, Qualification & Validation, you will be responsible for developing, leading and providing oversight to the commissioning, qualification and validation (CQV) activities for Capital Projects, and Continuous Lifecycle Verification within PDx segment of GE Healthcare. The role involves ensuring, that PDx has appropriate business processes in place to ensure our facilities and equipment can be properly commissioned and validated to meet business and regulatory requirements. They shall lead the business transformation across our sites as we transition to a Lean Risk based CQV for manufacturing and associated computer systems validation within a Digitized C&Q Platform. They shall work closely with site CQV Leaders and interface with Functions, (Project Management, Quality, Engineering, Lean & Digital and EHS) as well as External Project Partners (Engineering, Construction Management and Qualification Service Providers) to ensure successful implementation of a Lean CQV strategy on project delivery and in continuous operations.

Job Description

Responsibilities

  • Lead delivery of CQV for the PDx portfolio of projects across our Contrast Media and Molecular Imaging to ensure successful delivery of capital projects, safely, to the right quality within cost and schedule constraints.

  • Ensure robust and Lean Commissioning & Qualification systems, Site Master Validation plans, methods and tools in place for operational Lifecycle and Continuous Verification C&Q on sites.

  • Drive the adoption of Risk based Commissioning & Qualification and implement continuous improvements and innovations to ensure PDx is aligned with best practice and latest regulatory requirements.

  • Drive the transformational rollout, implementation and adoption of digitized C&Q

  • Lead implementation of Computer Systems Validation for Manufacturing Facilities on our sites and supporting Process Automation systems

  • Credibly present and defend the validation status as appropriate to external and internal auditors and agencies.

  • Ensure on projects, the creation and implementation of appropriate CQV strategy and project planning and resourcing, aligned with design and construction sequencing and key functions.

  • Lead stage gate reviews of projects in planning and execution phases to ensure strategy, timelines, sequences, resources are optimised for successful project delivery

  • Ensure on projects that an appropriate handover strategy to end users is developed and ultimately delivered. This shall include training, document handover, operation strategy.

  • Develop the CQV network and capabilities across PDx

Required Qualifications

  • Relevant qualification (Degree) and significant experience in pharmaceutical industry commissioning and qualifying GXP systems.

  • Certification in project management (PMP or equivalent) is a plus.

Desired Characteristics

  • Proven track record of managing large-scale C&Q programs from design phase through to closeout and handover.

  • Multi-regional / Global experience

  • Global and enterprise-wide mentality coupled with strong communication skills (verbal & written), and the ability to articulate ideas to influence different levels of leadership ensuring alignment of C&Q methodologies across projects and sectors

  • Proven knowledge of C&Q methodologies and the current industry requirements

  • Experience in the deployment and/or extensive working knowledge/ experience of a digitized C&Q platform.

  • Clear understanding of regulatory requirements for EU, China and US regulatory bodies in particular ensuring CQV is delivered meeting all regulatory requirements and guidelines.

  • Strong analytical problem-solving skills, strategic decision maker, effective planner, and ability to communicate effectively.

  • Strong capability to collaborate with and influence technical leaders across different PDx segments and functions, as well as external project partners (Engineering, Construction firms, C&Q partners, etc.)

  • Location Cork, Lindesnes, Oslo. Mix of On site and hybrid

  • Some International travel is likely in this role potentially including weekends and multi-week stays. Travel of approximately up to 20% away from home

Inclusion and Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Behaviors

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

#LI-BG1
#LI-onsite

    Additional Information

    Relocation Assistance Provided: No

    Locations

    • Global

    Salary

    Estimated Salary Rangemedium confidence

    120,000 - 200,000 USD / yearly

    * This is an estimated range based on market data and may vary based on experience and qualifications.

    Skills Required

    • Commissioning, Qualification & Validation (CQV)intermediate
    • Risk-based CQV methodologiesintermediate
    • Computer Systems Validationintermediate
    • Project managementintermediate
    • Regulatory compliance (EU, China, US)intermediate
    • Lean transformationintermediate

    Required Qualifications

    • Relevant degree and significant experience in pharmaceutical CQV for GXP systems (experience)
    • PMP or equivalent certification (plus) (experience)

    Responsibilities

    • Lead CQV delivery for PDx capital projects
    • Ensure Lean CQV systems and Site Master Validation plans
    • Drive adoption of risk-based CQV and digitized platforms
    • Implement Computer Systems Validation
    • Present validation status to auditors
    • Lead stage gate reviews and handover strategies

    Benefits

    • general: Competitive salary and benefits
    • general: Career opportunities
    • general: Culture fostering care, collaboration and support

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    GE Healthcare logo

    Global Head Commissioning, Qualification & Validation (CQV)

    GE Healthcare

    Engineering Jobs

    Global Head Commissioning, Qualification & Validation (CQV)

    full-timePosted: Jan 14, 2026

    Job Description

    Job Description Summary

    As the Global Head of Commissioning, Qualification & Validation, you will be responsible for developing, leading and providing oversight to the commissioning, qualification and validation (CQV) activities for Capital Projects, and Continuous Lifecycle Verification within PDx segment of GE Healthcare. The role involves ensuring, that PDx has appropriate business processes in place to ensure our facilities and equipment can be properly commissioned and validated to meet business and regulatory requirements. They shall lead the business transformation across our sites as we transition to a Lean Risk based CQV for manufacturing and associated computer systems validation within a Digitized C&Q Platform. They shall work closely with site CQV Leaders and interface with Functions, (Project Management, Quality, Engineering, Lean & Digital and EHS) as well as External Project Partners (Engineering, Construction Management and Qualification Service Providers) to ensure successful implementation of a Lean CQV strategy on project delivery and in continuous operations.

    Job Description

    Responsibilities

    • Lead delivery of CQV for the PDx portfolio of projects across our Contrast Media and Molecular Imaging to ensure successful delivery of capital projects, safely, to the right quality within cost and schedule constraints.

    • Ensure robust and Lean Commissioning & Qualification systems, Site Master Validation plans, methods and tools in place for operational Lifecycle and Continuous Verification C&Q on sites.

    • Drive the adoption of Risk based Commissioning & Qualification and implement continuous improvements and innovations to ensure PDx is aligned with best practice and latest regulatory requirements.

    • Drive the transformational rollout, implementation and adoption of digitized C&Q

    • Lead implementation of Computer Systems Validation for Manufacturing Facilities on our sites and supporting Process Automation systems

    • Credibly present and defend the validation status as appropriate to external and internal auditors and agencies.

    • Ensure on projects, the creation and implementation of appropriate CQV strategy and project planning and resourcing, aligned with design and construction sequencing and key functions.

    • Lead stage gate reviews of projects in planning and execution phases to ensure strategy, timelines, sequences, resources are optimised for successful project delivery

    • Ensure on projects that an appropriate handover strategy to end users is developed and ultimately delivered. This shall include training, document handover, operation strategy.

    • Develop the CQV network and capabilities across PDx

    Required Qualifications

    • Relevant qualification (Degree) and significant experience in pharmaceutical industry commissioning and qualifying GXP systems.

    • Certification in project management (PMP or equivalent) is a plus.

    Desired Characteristics

    • Proven track record of managing large-scale C&Q programs from design phase through to closeout and handover.

    • Multi-regional / Global experience

    • Global and enterprise-wide mentality coupled with strong communication skills (verbal & written), and the ability to articulate ideas to influence different levels of leadership ensuring alignment of C&Q methodologies across projects and sectors

    • Proven knowledge of C&Q methodologies and the current industry requirements

    • Experience in the deployment and/or extensive working knowledge/ experience of a digitized C&Q platform.

    • Clear understanding of regulatory requirements for EU, China and US regulatory bodies in particular ensuring CQV is delivered meeting all regulatory requirements and guidelines.

    • Strong analytical problem-solving skills, strategic decision maker, effective planner, and ability to communicate effectively.

    • Strong capability to collaborate with and influence technical leaders across different PDx segments and functions, as well as external project partners (Engineering, Construction firms, C&Q partners, etc.)

    • Location Cork, Lindesnes, Oslo. Mix of On site and hybrid

    • Some International travel is likely in this role potentially including weekends and multi-week stays. Travel of approximately up to 20% away from home

    Inclusion and Diversity

    GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

    Behaviors

    We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

    Total Rewards

    Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

    #LI-BG1
    #LI-onsite

      Additional Information

      Relocation Assistance Provided: No

      Locations

      • Global

      Salary

      Estimated Salary Rangemedium confidence

      120,000 - 200,000 USD / yearly

      * This is an estimated range based on market data and may vary based on experience and qualifications.

      Skills Required

      • Commissioning, Qualification & Validation (CQV)intermediate
      • Risk-based CQV methodologiesintermediate
      • Computer Systems Validationintermediate
      • Project managementintermediate
      • Regulatory compliance (EU, China, US)intermediate
      • Lean transformationintermediate

      Required Qualifications

      • Relevant degree and significant experience in pharmaceutical CQV for GXP systems (experience)
      • PMP or equivalent certification (plus) (experience)

      Responsibilities

      • Lead CQV delivery for PDx capital projects
      • Ensure Lean CQV systems and Site Master Validation plans
      • Drive adoption of risk-based CQV and digitized platforms
      • Implement Computer Systems Validation
      • Present validation status to auditors
      • Lead stage gate reviews and handover strategies

      Benefits

      • general: Competitive salary and benefits
      • general: Career opportunities
      • general: Culture fostering care, collaboration and support

      Target Your Resume for "Global Head Commissioning, Qualification & Validation (CQV)" , GE Healthcare

      Get personalized recommendations to optimize your resume specifically for Global Head Commissioning, Qualification & Validation (CQV). Takes only 15 seconds!

      AI-powered keyword optimization
      Skills matching & gap analysis
      Experience alignment suggestions

      Check Your ATS Score for "Global Head Commissioning, Qualification & Validation (CQV)" , GE Healthcare

      Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

      ATS compatibility check
      Keyword optimization analysis
      Skill matching & gap identification
      Format & readability score

      Answer 10 quick questions to check your fit for Global Head Commissioning, Qualification & Validation (CQV) @ GE Healthcare.

      Quiz Challenge
      10 Questions
      ~2 Minutes
      Instant Score

      Related Books and Jobs

      No related jobs found at the moment.