Global C&Q Director

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 specific unit operations and platforms - drug substance/primary, DP/sterile filling, and packaging.

• Strong project management skills, with experience in managing complex, multi-site projects.

• Deep and broad understanding of the capital project lifecycle - design, construction, commissioning, qualification, to operation.

• Strong stakeholder management and influencing capabilities

• Leadership skills that enable the introduction of new ways of working and accelerated change management.

• Must be able to interact well with peers, subordinates, and senior personnel in scientific, engineering, and operational disciplines.

• Demonstrated ability to participate as a leader or member on cross-functional and self-directed work teams.

• Must be comfortable and thrive in ambiguity and think strategically to solve complex problems.

• Masters in Engineering, Professional Engineer, MBA, CSP, or PMP.

• Collaboration and participation in industry best-practice guidelines and knowledge sharing groups.

• Excellent 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 contracts

• Familiar with the GCP Project Management Framework (PMF), relevant engineering standards and compliance requirement as well as Quality Management Systems

Please 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.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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 UKRecruitment.Adjustments@gsk.com 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. Click the link and scroll to the Careers Section where you will find answers to multiple questions we receive

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/