Packaging Material And Equipment Technologist

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 The Packaging Material and Equipment Technologist will provide hands-on technical delivery for packaging activities within the Worthing Site Packaging Project. Reporting to the Packaging Technology Project Lead, the role will assess and implement primary, secondary and tertiary packaging materials; define and execute trials; support material and equipment qualification and validation; complete technical risk assessments; and create or update specifications, drawings and artwork inputs through formal change control. A central requirement is to understand how material properties, pack design and print or coding requirements interact with forming, sealing, handling, inspection and cartoning equipment so that solutions are robust, compliant and capable at production scale. The role will work through a cross-functional matrix with MSAT, Engineering, Operations, Quality, Regulatory, Artwork Packaging Services, Supply Chain and external material and equipment suppliers. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: •

Plan and complete assigned material, component and equipment-interface activities for primary, secondary and tertiary packaging, from development and approval through line introduction and routine manufacture, maintaining clear evidence and escalating risks or dependencies. •

Evaluate how material properties, tolerances, pack design and print or coding requirements affect forming, sealing, feeding, handling, coding, vision inspection and cartoning; define appropriate machine settings, operating ranges and controls. •

Develop and execute trial, qualification and validation protocols for packaging materials, pack formats and equipment interfaces, including objectives, sampling plans and acceptance criteria; analyse results, resolve deviations and document evidence-based conclusions. •

Lead or contribute to technical risk assessments, FMEA, transit assessments where applicable; troubleshoot performance issues, support root-cause investigations and translate identified risks into proportionate controls, test plans and corrective actions. •

Create, review and update component specifications, drawings, artwork briefs, master data, protocols, reports and change-control records, ensuring alignment with approved pack requirements, market needs, GMP and regulatory expectations and maintaining inspection-ready traceability. •

Knowledge of primary, secondary and tertiary packaging materials, component manufacture and printing techniques, with a strong understanding of how material properties and tolerances influence forming, sealing, feeding, coding, online artwork printing, inspection, handling and line performance. •

Demonstrated experience planning, executing, analysing and reporting material, process or equipment trials, qualification and validation using scientifically sound, risk-based approaches. •

Experience applying Quality by Design, FMEA, root-cause analysis and technical risk assessment, with the ability to interpret trial and production data, identify trends or failure modes and convert evidence into practical controls and recommendations. •

Experience creating or updating packaging specifications, technical drawings, artwork inputs and controlled records through formal change control, underpinned by good working knowledge of GMP, data integrity, product quality and regulatory requirements. •

CMC Strategy, Data-Driven Decision Making, Data Integrity, Debate Moderation, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Process Optimization, Project Leadership, Risk Awareness, Scientific Writing, Technology Transfer

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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