NPI Launch Lead in Barnard Castle

GSK Barnard Castle is a key secondary manufacturing site and has invested heavily in industry 4.0 state of the art, bespoke equipment to support sustained new product introductions and volume increases. As a key supplier of some of GSK's blockbuster products, the site contributes revenues of ~$2Bn annually. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.

As an NPI Launch Lead at GSK Barnard Castle you will own and drive logistics for pre‑agreed pharmaceutical and major consumer product launches—including transfers‑in, line extensions and in‑licensing deals—leading Logistics project management for defined new business projects and overseeing development and clinical trial supplies. As Lead for assigned launches you will be the single point of contact for launch planning, preparing launch scenarios and aligning on‑site and off‑site stakeholders to meet initial wave‑1 timelines and subsequent wave‑2 market rollouts, while ensuring GMP, Quality, EHS and regulatory requirements are met and commercial and operational risks are identified and managed to deliver timely, compliant and commercially successful product introductions.

In this role you will:

• Lead and coordinate site launch activities for revenue- and medically-critical products across Pharma (HIV, Oncology, Immuno‑inflammation, Respiratory) and Consumer franchises, managing phased launches (main markets, wave 1 and 2) to Global markets and third parties as required.
• Direct cross-functional, multi-level project teams and engage internal (Regulatory, SLDC, Validation, Planning), off-site (print/component suppliers, Hubs/LOC supply planners) and external launch teams to execute product launch plans and handovers to business-as-usual.
• Develop, maintain and communicate detailed launch plans (including changes), oversee scheduling of development/clinical batches in SAP, provide GMM data and manage the CT order book with R&D and other off-site stakeholders.
• Manage packaging and registration deliverables to meet timelines: registration sample project management, pack graphic design templates, brochures, and creation/supply of registration packs to minimise registration timelines.
• Represent launches in key site governance (Value Stream OFM, Schedule Lock, Planner Handover, Capacity Review), establish capacity inputs for SRM/LRF, agree handover timing with Global Planning, and lead After Action Reviews post-launch.
• Ensure audit readiness, regulatory and quality compliance at all times through audit fronting, self-inspection support, problem solving and implementation of corrective actions; build and maintain effective stakeholder relationships (MPD, GMS Strategy, Global Logistics/Planning, Regulatory) to secure engagement.

Basic Qualifications & Skills:

• GCSEs including Maths and English.
• Experience in logistics scheduling/planning/material management and SAP (PE modules).
• Experience working in a complex matrix environment and with product/pack launch processes.
• Knowledge of logistics/supply chain and strong project management capability.
• Significant experience in a pharmaceutical environment, ideally across multiple functions.
• Proficiency in MS Office (Word, Excel, Project, PowerPoint).

Preferred Qualifications:

• Business or Science qualification such as a Bachelor's degree (or equivalent).
• Specialisation in Supply Chain.
• Broader supply chain exposure across multiple disciplines (planning, scheduling, project management).
• Experience partnering across internal and external stakeholder groups (e.g., Global Planning, Regulatory, Validation, hubs, LOCs).

Closing Date for Applications: 6th February 2026 (COB)

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.

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. 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.