Global Commissioning & Qualification (C&Q) DirectorThis role will preferably be based at GSK HQ, UK but can be based at other European strategic locations on a case-by-case basis.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 geographiesThe 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.In this role you will: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.Stakeholder Management:Build and maintain strong relationships with internal and external stakeholders, including suppliers, contractors, and regulatory agencies.Why you?Basic Qualifications & Skills:We are looking for professionals with these required skills to achieve our goals:BSc in relevant discipline/Chartered Engineer.Significant experience in commissioning, qualification, and validation within the pharmaceutical or biopharmaceutical industry.Proven track record of successfully leading and managing global C&Q projects across all geographies.In-depth knowledge of regulatory requirements and industry standards (e.g., GMP, GAMP, ICH guidelines).Strong project management skills, with experience in managing complex, multi-site projects.Strong stakeholder management and influencing capabilitiesPreferred Qualifications & Skills:Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:MSc or PhD or other Chartered / Professional Qualification in a relevant disciplineExcellent management, communication and interpersonal skills, with comfort cooperating with individuals internally and externally at all organisational levels.Understanding of how different functions interface on GSK projects.Solid knowledge of GSK project process, User requirement management, quality and compliance requirement, site project completion and pre-start processes, and how these impact engineering and design, construction, commissioning, and qualification contractsFamiliar with the GCP Project Management Framework (PMF), relevant engineering standards and compliance requirement as well as Quality Management SystemsClosing Date for Applications – 16th June 2025Please take a copy of the Job Description, as this will not be available post closure of the advert.
When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.We make and supply medicines and vaccines all around the globe and our teams own every production stage, from creating quality products at our manufacturing sites to designing effective supply forecasting and regulatory inspections; all powered by digital, data and analytics. We operate at impressive scale, producing over 2.3 billion packs of medicines and doses of vaccines in 2023.We continue to modernise, so we can launch even more new products at speed whilst continuing to deliver across our entire portfolio through our relentless focus on quality, safety, and service. The way we work will change. For some, the shift in technology and products will be revolutionary. Our R&D pipeline demands a new kind of supply chain, and we need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients.If you are interested in joining us, find out more:Why GSK?Uniting science, technology and talent to get ahead of disease together.GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on or 0808 234 4391. The helpline is available from 8.30am to 12.00 noon Monday to Friday, during bank holidays these times and days may vary.Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a UK Recruitment FAQ guide. 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