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

If you have the following characteristics, it would be a plus:

Previous experience in the pharmaceutical, healthcare, or life sciences industry.

Familiarity with quality management systems, regulatory requirements or audit processes.

Experience using project management tools or software.

Strong problem-solving skills and attention to detail.

Comfortable working independently and as part of a team.

Commitment to fostering an inclusive work environment where every voice is heard.

Location

This role is based on-site in the United Kingdom at our Worthing Site.

About Worthing Manufacturing Site:

Manufacturing at the Worthing site is for antibiotics (Penicillin). It is advised that you take this into consideration when deciding to apply for this position.

GSK Worthing Site is a mixed manufacturing site with complex regulatory pressures. Manufacturing processes are highly technical and include high hazard activities.

What we offer you

You will join a team committed to safety, high standards and practical learning. You will have opportunities to build supervisory and technical skills. You will work with cross-functional partners and contribute to improving processes that matter to patients worldwide. We encourage applications from people at different career stages and backgrounds. If you are motivated to lead, learn and make a tangible impact, please apply now.

Skills

Data Integrity, Detail-Oriented, Digital Fluency, Emergency Response, Financial Acumen, GxP Regulations, Lean Management, Manufacturing Processes, Problem Solving, Production Management, Project Coordination, Quality Compliance, Regulatory Compliance, Risk Awareness, Site Operations

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 at UKRecruitment.Adjustments@gsk.com 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

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