Tablet Packaging Compliance & Project Support

Tablet Packaging Compliance & Project Support Closing Date: 2nd November 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 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. 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. Position Summary You will play a vital role in supporting our compliance and project activities with accuracy and a strong attention to detail. This role requires you to work closely with teams across the business to ensure processes run smoothly and meet all compliance standards. We value candidates who are organised, proactive, and enjoy working collaboratively to solve challenges. Joining us means contributing to a purpose-driven mission where your work helps unite science, technology and talent to get ahead of disease together. This role offers an exciting opportunity to grow your skills while making a meaningful impact.   Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: • Own and drive the function audit universe and audit readiness programme, including Facility and Equipment GEMBA schedules, follow-up actions, and acting as primary contact for inspection readiness activities. • Define, own and drive continuous improvement programmes and deviations for compliance (including the function Data Integrity plan) and lead daily compliance meetings to generate, review and act on data and frameworks to drive efficiencies and sustain performance. • Own Quality boards and generate the Monthly Quality pack for technicians/TLs, using recent issues, actions and quality bulletins to challenge existing standards and ways of working to improve compliance, efficiency and robustness. Lead the 5S deployment across the floor. • Act as the customer for all non–self-delivered projects within the function, ensuring project delivery (equipment, systems and processes) is appropriate for use in production and meets operational requirements, priorities and functional needs. • Ensure training plans for new equipment and new/updated GMP documentation (SOP, SWI etc.) are fit for purpose, enable technicians to perform their roles compliantly, support seamless integration from installation to steady-state production, and are reviewed periodically on time. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: • A bachelor’s degree or equivalent experience in a relevant field such as life sciences, business administration, or compliance. • Experience supporting compliance or project management activities in a regulated environment. • Strong organisational skills with the ability to manage multiple tasks and deadlines effectively. • Excellent written and verbal communication skills in English. Proficiency in common office applications such as MS Word, Excel, and PowerPoint. • Ability to work on-site in the United Kingdom, with hybrid working options considered. Preferred Qualification