At a Glance
- Tasks: Manage and improve stability data for small molecule studies while collaborating with cross-functional teams.
- Company: Join a leading pharmaceutical company committed to innovation and quality.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Dynamic role with opportunities for digital tool adoption and process improvement.
- Why this job: Make a real impact in drug development and enhance your analytical skills.
- Qualifications: Bachelor’s degree in a scientific field and experience in regulated environments.
The predicted salary is between 35000 - 45000 £ per year.
Role Overview
You will manage and improve stability data for small molecule studies. You will create and maintain study protocols, collect and analyze 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 and work closely with cross‑functional colleagues, external partners and quality teams.
Responsibilities
- 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
- 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
- Experience with stability management or laboratory information systems e.g., 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)
Scientist, Analytical Operations - Small Molecule Stability Data Management in Stevenage employer: GlaxoSmithKline
At GSK, we pride ourselves on being an exceptional employer, offering a collaborative work culture that fosters innovation and professional growth. Our commitment to employee development is reflected in our comprehensive training programmes and opportunities for cross-functional collaboration, particularly in our vibrant location where cutting-edge research meets regulatory excellence. Join us to be part of a team that values your contributions and supports your career aspirations in the dynamic field of analytical operations.
