Scientist, Analytical Operations Small Molecule Stability Data Management

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Scientist Analytical Operations - Small Molecule Stability Data Management

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

Why you

Basic Qualifications & Skills:

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

• Bachelors 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 if you do not have them please still apply:

• 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)

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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 cover letter and CV will be used to assess your application.

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 peoples fosters a culture ambitious for patients accountable for impact and committed to doing the right thing making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science technology and talent to get ahead of disease together.

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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 were 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.

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