Latest IT Recruitment Jobs

Regional EM Engineering Lead

This role involves ensuring strong engineering performance at Contract Manufacturing Organization (CMO) sites, supporting new product introductions, and managing engineering programs for Large Molecule Drug Substance. The position requires expertise in engineering aspects of large molecule drug substance and involves site assessments, capital management, and troubleshooting.

GSK

On-site Permanent

Specialist - Extractables and Leachable - MSAT EM

This role involves working with internal and external labs to ensure E&L testing is completed scientifically and compliantly. Responsibilities include conducting risk assessments, delivering technical information, and managing risk escalation for biopharmaceutical manufacturing processes and packaging systems.

GSK £70,650 – £117,750 pa

On-site Permanent

Associate Director Integrated Bioanalysis – Biopharma Bioanalytical Program Lead

This role involves leading the bioanalytical strategy for diverse therapeutic modalities, collaborating with global project teams to develop robust assays, and translating complex data into clear program decisions. The position is highly visible, requiring cross-functional influence and external representation of scientific findings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Scientist, Bioconjugation

This role involves designing and conducting bioconjugation experiments to support oncology drug discovery, with a focus on conjugating small molecules to antibodies and related scaffolds. The scientist will characterise bioconjugates using HPLC, LC-MS, and other analytical techniques, optimise conjugation strategies, and contribute data-driven insights to early-stage research programmes. The position requires strong technical expertise in protein chemistry and robust laboratory practices within a collaborative, multidisciplinary environment.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for regulatory and research purposes. Working closely with statisticians and data scientists, the role involves developing validated datasets, tables, listings, and figures using CDISC standards such as SDTM and ADaM, while ensuring compliance with GxP and ICH guidelines. The position supports agile delivery within a hybrid work environment and emphasizes technical excellence, collaboration, and innovation in clinical data programming.

GSK Stevenage, United Kingdom

Hybrid Permanent

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in team efficiency and transparency.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Programmer / Analyst

The Principal Programmer / Analyst role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering innovation and quality assurance in a global, agile environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Principal Scientist/Senior Principal Scientist – Statistical Genetics

This role involves applying advanced statistical and computational methods to large-scale genetic, genomic, and clinical datasets to drive insights in drug discovery and development. The scientist will work across therapeutic areas to interpret causal disease mechanisms, support target and biomarker identification, and enable precision medicine strategies within a collaborative, multidisciplinary R&D environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data governance, system ownership, and digital integration. The individual will ensure data integrity, drive compliance with regulatory requirements like Transfer of Value, and translate operational needs into scalable digital solutions. Working across cross-functional teams, they will enhance efficiency, quality, and transparency in clinical operations through robust dashboards, automation, and process improvements.

GSK Stevenage, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies, ensuring data integrity, system performance, and compliance. The individual will lead data governance, dashboard development, and system integration—particularly for platforms like Veeva and IdeaPoint—while acting as a bridge between business and technology teams to drive efficiency and compliance in clinical study delivery.

GSK London, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Project Specialist (External Manufacturing-Drug Product)

This role involves managing technology transfer projects for external contract manufacturing organizations (CMOs) in the pharmaceutical sector, ensuring alignment between GSK and suppliers on timelines, quality, and technical deliverables. The specialist will coordinate cross-functionally across procurement, quality, technical, and supply teams to operationalize new assets or suppliers, with a focus on sterile drug products like monoclonal antibodies and vaccines. Key responsibilities include maintaining critical path schedules, mitigating risks, and driving project governance from transfer through to product launch.

GSK Worthing, United Kingdom €69,600 – €116,000 pa

Hybrid Permanent