Global C&Q Director

Job description

Site Name: GSK HQ, Belgium‑Wavre, Italy - Parma, Rosia, UK - Angus - Montrose, UK - County Durham - Barnard Castle, UK - North Ayrshire - Irvine

Posted Date: Dec 17 2025

GSK remains committed to achieving bold commercial ambitions for the future. By 2031, we aim to deliver £40 billion in annual sales, leveraging our existing strong performance momentum to significantly increase our positive impact on the health of billions of patients globally. Our Ahead Together strategy is centred on early intervention to prevent and alter the course of disease, thereby protecting people and supporting healthcare systems.

Our diverse portfolio consists of vaccines, specialty medicines, and general medicines. Through continuous innovation and a dedicated focus on scientific and technical excellence, we strive to develop and launch new, groundbreaking treatments that address critical health challenges.

The Global C&Q Director will lead and manage the consistent deployment of best in class capability and capacity of commissioning and qualification activities within the project portfolio under the accountability of Global Capital Projects group (GCP). This role is responsible for ensuring that all project equipment, systems, and processes consistently meet regulatory and company standards to ensure product quality and patient safety.

The Global C&Q Director will work closely with cross-functional teams, including engineering, quality assurance, manufacturing, and regulatory affairs, to ensure the delivery of compliant and efficient commissioning and qualification programs. They will work to establish strong partnerships for efficient deployment of C&Q capability and resources across all geographies.

The Global C&Q Director will drive towards best in class practices leveraging digital and AI to continuously improve and drive superior performance within commissioning and qualification of large capital projects.

• Leadership and Strategy:
  • Support the development and implement global C&Q strategies, policies, and procedures based on company standards and prevailing regulations.
  • Provide leadership and direction to regional/project C&Q teams to ensure consistent application of standards and practices.
  • Collaborate with senior management to align C&Q activities with business objectives and regulatory requirements.
• Project Management:
  • Oversee the planning, execution, and completion of C&Q projects across multiple projects.
  • Ensure projects are delivered on time, within budget, and in compliance with regulatory standards.
• Technical Expertise:
  • Provide technical guidance and support for C&Q activities, including risk assessments, protocol development, and execution.
• Quality and Compliance:
  • Ensure that all C&Q activities comply with GSK's quality management system and applicable regulatory requirements (e.g., FDA, EMA, MHRA).
  • Implement continuous improvement initiatives to enhance C&Q processes and outcomes.
• Team Development:
  • Support the recruitment, training, and mentoring of C&Q staff to build a high‑performing global team.
  • Conduct performance evaluations and provide feedback to support professional growth.
  • Be a global team ambassador to the local site project environment.
  • Act as a visible advocate for diversity in engineering and project delivery.
  • Act as a visible advocate for GSK Safety Life Saving Rules.
• Stakeholder Management:
  • Build and maintain strong relationships with internal and external stakeholders, including suppliers, contractors, and regulatory agencies.

• Engineering degree (Mechanical, Electrical, Chemical, Civil/Structural).
• Extensive project validation experience and proven experience in leading validation teams in pharmaceutical or biotech industry.
• Proven track record of successfully leading and managing global C&Q projects across all geographies and end‑to‑end.
• Proven track record of regulatory authority audit participation and defence of validation project plans and results.
• In‑depth knowledge of regulatory requirements and industry standards (e.g., GMP, GAMP, ICH guidelines).
• Experience in biopharm…