Tablet Packaging Documentation Specialist – 12 Month SecondmentFTC

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We manufacture and supply reliable high-quality medicines and vaccines to meetpatientsneeds 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;itsvital 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.

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AsTablet Packaging Documentation Specialistyou will owngovernand continuously improve the tablet packaging Batch Production Record (BPR) system for oral solid dose products ensuring compliance with updated global packaging standards GMP requirements data integrityprinciplesand document management processes.

The role is accountable for the designimplementationand lifecycle management of hybrid MERP/Veeva batch documentation supporting right-first-time batch execution effective implementation of artwork and process changes regulatorycomplianceand sustained inspection readiness.

In this role you will

• Lead the designimplementationand lifecycle management of tablet packaging Batch Production Records (BPRs) ensuring alignment with global packaging standards and site quality requirements.

• Own the transition and ongoing governance of SKU-specific packaging documentationestablishingstandardised and scalable documentation structures that support business and complianceobjectives.

• Developmaintainand continuously improve hybrid MERP and Veeva batch documentation ensuring documentationremainscurrentaccurateand compliant with GMP data integrity and document management requirements.

• Coordinate cross-functional review and approval of new and revised packaging documentation with Operations MSAT QA QP Supply Chain Artwork and E2E stakeholders.

• Assesscoordinateand implement documentation changes arising from artwork updates regulatory requirements processimprovementsand business initiatives ensuring effective change control and minimal impact to supply continuity.

• Maintain documentation structures and master datato support packaging execution traceabilityreconciliationand compliant batch release activities.

• Act as the Site Subject Matter Expert for tablet packaging documentation providing technical leadership training coaching and day-to-day support to operational teams and stakeholders.

• Conduct risk and impact assessments associated with packaging documentation changes ensuring quality patientcomplianceand business risks are appropriately managed and mitigated.

• Drive continuous improvement of packaging documentation processes using operational performance data deviationtrendsand user feedback to improve document effectiveness and right-first-time performance.

• Support audit and inspection readiness activities ensuring packaging documentation systems processes and proceduresremaincompliant with GMP Data Integrity and Regulatory requirements.

Why you

Basic Qualifications & Skills:

We are looking for professionals with these required skills to achieve our goals:

• Degree in a Scientific Engineering Pharmaceutical or related discipline; orequivalent experience gained within a pharmaceutical manufacturing environment.

• Experience working within a GMP-regulated pharmaceutical or highly regulated manufacturing environment.

• Strong understanding of batch production records packagingoperationsand documentation management processes.

• Knowledge of GMP requirements data integrityprinciplesand quality systems.

• Experience using electronic manufacturing and documentation systems such as MERP SAP Veeva Vault or equivalent platforms.

• Ability to manage complex documentation changes across multiple stakeholders and functions.

• Strong communicationinfluencingand stakeholder management skills.

• Demonstrated problem-solving and continuous improvement capability.

• management systems (e.g. ISO 9001).

Preferred:

• Experience of packaging artwork management and overprint processes.

• Understanding of batch reconciliation and packaging compliance requirements.

• Experience supporting regulatory inspections and audits.

• Knowledge of LeanGPSand continuous improvement methodologies.

• Project or change management experience.

Closing Date for Applications:18thAugust2026(COB)

Please take a copy of the Job Description as this will not be available post closure of the advert.

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 coverletterand CV will be used to assess your application.

We are addressing gender equality at all levels within ourorganisationwe alsoremaincommitted to improving ethnic diversity within GSK and recruiting and developing talent that mirrors the communities in which we work. With support from our Global Disability Council and our employee resource group the Disability Confidence Network we are working hard to create an inclusive workplace.

We want GSK to be somewhere everyone can feel a sense of belonging and thrive. Our success absolutely depends on our people.