Latest Healthcare Jobs

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leading the implementation of Medical Affairs processes, and supporting data generation across the EU and International regions. The role requires strong project management skills, knowledge of HIV, and the ability to work independently and collaboratively with diverse teams.

GSK

On-site Permanent

Regional Medical Advisor

The EU and International Regional Medical Advisor role involves representing the business voice, leveraging medical platforms, and aligning medical affairs processes across the EU and International regions. Responsibilities include supporting transversal business prioritization, improving communication with local operating companies, and assisting with data generation processes and investigator-sponsored studies.

GSK

On-site Permanent

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, focusing on generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna

On-site Contract

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Engineering Technician

The Engineering Technician role involves providing comprehensive engineering support for the Steriles Business Unit, focusing on equipment maintenance, GMP compliance, and continuous improvement initiatives. Responsibilities include breakdown repairs, calibration, quality documentation, and project support, all while maintaining high safety and regulatory standards.

GSK Barnard Castle, United Kingdom

On-site Permanent Shift-work

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

Process Engineer

The Process Engineer role involves providing technical expertise to support safe and efficient manufacturing at GSK's Montrose site. Responsibilities include resolving technical issues, contributing to capital projects, improving process plant software, and collaborating with cross-functional teams to ensure compliance and process improvements.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

On-site Contract

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

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, shaping development and approval pathways across international markets. Works at the intersection of R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient access. Focuses on solving complex regulatory challenges, mentoring talent, and improving processes to support long-term product success.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Process Technologist

As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.

GSK Barnard Castle, United Kingdom

On-site Permanent

Operational Technologist

This role involves providing real-time technical support for manufacturing operations, troubleshooting process issues, and driving continuous improvements in a regulated pharmaceutical environment. The technologist will work hands-on on the shop floor to ensure production efficiency, compliance, and product quality, while collaborating with cross-functional teams including engineering, quality, and production. Emphasis is placed on data-driven problem solving, maintaining audit readiness, and coaching frontline staff in GMP and technical standards.

GSK Barnard Castle, United Kingdom

On-site Permanent

Steriles Business Change Lead

Lead business change initiatives for sterile manufacturing at a GSK site in Barnard Castle, ensuring operational readiness across quality, compliance, and production systems. Coordinate cross-functional teams through commissioning, validation, and go-live phases, with a focus on safety, regulatory compliance, and sustainable performance improvement in a highly regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Steriles Standards Manager

Leads the development and enforcement of operational standards for sterile manufacturing, ensuring compliance with regulatory requirements and driving continuous improvement. Works cross-functionally with quality, engineering, and operations teams to standardize processes, support audit readiness, and strengthen control in aseptic environments. Focuses on reducing variability, improving compliance, and coaching teams in a highly regulated pharmaceutical setting.

GSK Barnard Castle, United Kingdom

On-site Permanent