Steriles Business Change Lead

Steriles Business Change Lead

Closing Date: 6th July 2026 (COB)

Business Introduction

We manufacture and supply reliable, high quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7billion packs of medicines and 409million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is vital to bringing our innovations to patients as quickly, efficiently and effectively. Technology is transforming how we manufacture, enabling us to increase speed, quality and scale of supply.

Position Summary

You will lead and shape business change for sterile manufacturing at a UK site. You will work across operations, engineering, quality and supply chain to design, plan and deliver change that improves safety, compliance and supply reliability. The role offers visible career growth, meaningful impact and the chance to help GSK unite science, technology and talent towards disease prevention.

Responsibilities

• Design, develop and implement the site operational readiness roadmap for the SLT, including milestones, readiness criteria, acceptance thresholds and functional alignment across QA, Operations, Engineering, IT, Supply Chain, Finance, HR and EHS.
• Act as the cross functional integrator, coordinating readiness across commissioning, operations, compliance, people, processes, systems, safety, permits, commercial arrangements and organisational change.
• Own the formal change control and governance process, including impact assessments, approvals, governance board updates, go/no go decisions, rollback planning and the site change management plan.
• Support commissioning, validation and sterile filling readiness, including IQ/OQ/PQ activities, water runs, media fills, PPQs, utilities, environmental monitoring and equipment readiness.
• Ensure documentation and compliance readiness by updating controlled document registers, SOPs, work instructions, validation master plans, asset registers, emergency plans and regulatory submissions in line with internal and external standards.
• Manage systems and data enablement, including CMMS/EAM, PLC/SCADA integration, MES, ERP, cybersecurity, access controls, data migration, asset hierarchies and system baselines.
• Confirm safe operations, campaign readiness and regulatory compliance, including cleaning/sterilisation procedures, gowning validation, alarm functionality, product mix planning, campaign schedules, changeovers, shift patterns, permits, licences, HAZOP/HAZID and safety submissions.
• Oversee post go live stabilisation with the SLT, monitoring reliability targets, process KPIs and operational performance, while supporting benefits realisation and ongoing enhancement after full operations go live.

Basic Qualification

• Significant experience working in sterile pharmaceutical manufacturing or aseptic processing environments.
• Proven experience leading change, projects or operational transformations in a regulated site.
• Strong stakeholder management and clear communication with operations, engineering and quality teams.
• Experience defining requirements, supporting testing and delivering readiness for production.
• Demonstrable focus on GMP, compliance and inspection readiness.
• Ability and willingness to work on site regularly and collaborate directly with shop floor teams.

Preferred Qualification

• Degree or vocational qualification in engineering, life sciences, manufacturing or a technical discipline.
• Experience with new product introductions, scale up, transfers or capital project delivery.
• Familiarity with continuous improvement methods such as Lean or Six Sigma.
• Knowledge of manufacturing execution systems or electronic batch records.
• Experience coaching frontline leaders and building operational capability.
• Track record of delivering benefits through structured change and measurement.

Working model

This role is on site at Barnard Castle. You should be prepared to spend significant time at the manufacturing site to lead activities and work directly with operational teams.

What we value in you

You are practical and calm under pressure, set clear expectations and support others to meet them. You act with integrity and put safety and quality first. You make decisions using evidence and welcome learning. You create an inclusive workplace where different perspectives are heard and respected.

Equal Opportunity Employer

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, military service or any other basis prohibited under federal, state or local law.