Scientist, Analytical Operations - Small Molecule Stability Data Management

This job is with GSK, an inclusive employer. We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

You will manage and improve stability data for small molecule studies. You will create and maintain study protocols, collect and analyse incoming datasets, and produce clear tables, summaries and visualisations for teams and regulatory submissions. You will contribute and drive process improvement through the adoption of digital tools. You will work closely with cross-functional colleagues, external partners and quality teams.

We value curiosity, care for data integrity and a practical approach to continuous improvement. This role offers clear career growth and the opportunity to make a meaningful impact on patient safety and product quality.

In this role you will:

• Create, review and maintain stability study protocols and schedules in line with regulatory and quality standards
• Collate stability data, perform trending and basic statistical analysis, and generate clear summaries and visualisations
• Maintain accurate study records and manage sample pull schedules across the study lifecycle
• Support audits and inspections through preparation of documentation and responses to quality queries
• Collaborate with internal teams and external partners to resolve issues and improve data processes
• Contribute to digital tool adoption and support data-driven workflow improvements

Basic Qualifications & Skills:

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

• Bachelor's degree in a scientific discipline (or equivalent experience)
• Experience working in a regulated environment (GMP, GxP or similar) with knowledge of data integrity principles and quality documentation standards
• Experience handling analytical datasets and preparing study summaries or reports
• Strong communication skills for effective reporting and stakeholder engagement

Preferred Qualifications & Skills:

Please note the following skills are not necessary, just preferred:

• Experience with stability management or laboratory information systems i.e., Labware CLS, LIMS
• Experience in small molecule development or analytical operations
• Exposure to regulatory submissions or inspections
• Understanding of statistical methods used in stability evaluation
• Experience driving process improvement or digital adoption and user acceptance testing
• Confidence using digital and data visualisation tools e.g., Statistica, Spotfire dashboards

Closing Date for Applications - 25th June 2026 (COB)

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, colour, 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.