Senior Project Manager (R&D Stream) – Capital Projects Engineering

GSK

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profile Job Location:

Ware - UK

profile Monthly Salary: Not Disclosed
Posted on: 3 days ago
Vacancies: 1 Vacancy

Job Summary

At GSK Ware the campus comprises both a manufacturing site (Global Supply Chain) and a Research & Development (R&D) site. The Capital Projects Engineering department is responsible for the management and delivery of capital portfolios spanning both sides of the campus.

We are seeking an experienced and proactive Senior Project Manager to join the Capital Projects Engineering Team at the GSK Ware site aligned specifically to the R&D Capital Portfolio. This role will take full accountability for the endtoend delivery of capital projects from inception and business case formation through design construction commissioning validation and handover following GSKs Project Management Framework (PMF) site standards and governance processes.

Projects may include:

  • New pharmaceutical production equipment (tablet presses packing lines bespoke blending and filling equipment)
  • Critical utilities and infrastructure (HV/LV power HVAC process utilities chilled water steam/condensate and technical services)
  • Modifications to R&D facilities and scientific workspaces
  • R&D equipment installations (e.g. containment equipment)

Key Responsibilities:

Project Management & Delivery

  • Lead the delivery of assigned capital projects within the R&D stream ensuring adherence to PMF cost schedule quality and safety requirements.
  • Conduct the Business Analysis phase defining business benefits assessing technical feasibility and developing appropriate solution options.
  • Prepare and submit Project Investment Proposals (PIPs) and supporting documentation to secure capital approval.
  • Develop and maintain key project documents including Charters User Requirement Briefs (URB) and User Requirement Specifications (URS) in partnership with end users validation and technical SMEs.
  • Facilitate design reviews HAZOPs safety studies GMP and quality reviews ensuring robust and compliant project design.

Scope & Change Management

  • Define clarify and agree project scope with stakeholders ensuring clear deliverables boundaries and acceptance criteria.
  • Maintain disciplined scope control throughout the lifecycle preventing scope creep and ensuring continued alignment to requirements.
  • Coordinate project change controls from generation through approval ensuring compliant documentation.

EHS Compliance & Governance

  • Ensure all project activities comply with GSK EHS standards CDM regulations and quality systems.
  • Develop PreConstruction Information (PCI) and comply with HSE requirements (e.g. F10 notifications).
  • Provide visible HSE management to ensure safe delivery within operational and R&D environments.

Execution Commissioning & Handover

  • Manage FATs/SATs equipment acceptance and integration into R&D environments.
  • Coordinate shutdowns downtime planning and operational impacts with science and production stakeholders.
  • Oversee commissioning qualification/validation activities and ensure complete technical documentation and handover packages.

Financial & Contract Management

  • Own project budgets including PIP allocations contingency management procurement activities and purchase order management.
  • Ensure robust cost forecasting reporting and alignment with financial governance requirements.
  • Generate clear scopes of work and support contract administration activities (e.g. NEC4 PSC and ECC).

Stakeholder & Partner Management

  • Act as the single point of accountability for project delivery working closely with the R&D stream Capital Delivery Partner technical teams and suppliers.
  • Liaise effectively with senior stakeholders and sponsors ensuring transparent communication and timely escalations.
  • Present project updates risks and proposals at governance forums.
  • Manage technical queries related to project scope and execution

Planning & Portfolio Support

  • Contribute to annual and multiyear capital planning providing estimates prioritisation insights and schedule forecasts.
  • Support role clarity and accountability across internal teams and subcontractors.
  • Provide daytoday support to the R&D Capital Stream Lead.

About You:

This role would suit a motivated resilient and solutionsfocused project professional with experience delivering capital projects in scientific pharmaceutical or regulated environments.
You will:

  • Be a qualified engineer (degree level or via professional registration).
  • Apply structured project management approaches risk management and governance discipline.
  • Build effective partnerships across internal and external stakeholders.
  • Demonstrate strong practical problemsolving abilities and manage multidisciplinary teams effectively.

About the Ware Site:

Ware is one of GSKs largest manufacturing and R&D sites home to circa 1500 employees. The site develops and launches new Oral Solid Dose (OSD) and Respiratory products while supporting highvolume global supply. As the only site responsible for launching the companys R&D pipeline for OSD products Ware plays a pivotal role in translating innovation into commercial success.

CLOSING DATE for applications: Friday 24th of April 2026 (COB).

Essential Qualifications:

  • Degreelevel qualification in Engineering (BEng/MEng) or a related technical discipline and/or professional registration (IEng/CEng) through a recognised engineering institution.
  • Significant experience delivering capital projects in a regulated scientific pharmaceutical or similarly complex technical environment including full lifecycle delivery (frontend design construction commissioning CQV and handover).
  • Demonstrated capability in scope cost schedule risk and change management for multidisciplinary projects including managing highcomplexity or highvalue capital works (e.g. 210mlevel projects).
  • Strong ability in contract administration and commercial frameworks ideally with experience in NEC4 PSC/ECC contracts.
  • Proven ability to navigate and apply quality validation EHS and compliance frameworks relevant to GMP/GxP and R&D environments.
  • Advanced stakeholder engagement and communication skills including confidence interacting with senior stakeholders sponsors and governance bodies.
  • Experience operating within a matrix organisation dealing with ambiguity priorities and timecritical decisionmaking.
  • Evidence of structured problemsolving capability and ability to manage/energise crossfunctional teams.

Desirable:

  • Formal project management accreditation (e.g. APM PMQ PRINCE2 Practitioner PMP).
  • Experience with GSKs PMF governance processes and capital investment frameworks.
  • Experience coordinating engineering change controls or technical change management in GxP environments (e.g. ECCs).
  • Strong familiarity with commissioning and validation documentation (e.g. URS IOQ/IOQ PCC/ECC packages).
  • Experience representing engineering or project delivery functions during audits or regulatory inspections

Benefits:

GSK offers competitive benefits including:

  • Competitive base salary and annual performance bonus
  • Professional development training and chartership support (IET IMechE IChemE etc.)
  • Opportunities to attend industry conferences
  • Access to health wellbeing and recognition programmes

If you would like to learn more about our company wide benefits and life at GSK we would suggest looking at our webpage Life at GSK GSK.

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 were 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 at where you can also request a call.

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 Recruitment FAQ guide. Click the link 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 GSKs 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 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 GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at Experience:

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At GSK Ware the campus comprises both a manufacturing site (Global Supply Chain) and a Research & Development (R&D) site. The Capital Projects Engineering department is responsible for the management and delivery of capital portfolios spanning both sides of the campus.We are seeking an experienced a...
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About us We are a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer. We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.

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