Latest Healthcare Jobs

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Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight in oncology clinical development, focusing on hematology. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It emphasizes physician leadership in trials from Phase I–III, with a strong focus on real-world impact and regulatory engagement.

GSK £222,750 – £371,250 pa
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Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight and clinical development for oncology and hematology programs, with responsibilities spanning study design, safety monitoring, data interpretation, and regulatory engagement. The Medical Director will collaborate with cross-functional teams and external experts to ensure clinical integrity and patient-centered decision-making in late-stage drug development. The position requires deep expertise in hematology-oncology and experience in Phase I–III trials within a pharmaceutical or biotech setting.

GSK PLN 455,250 – PLN 758,750 pa
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Senior Manager, Packaging Engineering

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.

Moderna Oxford, United Kingdom
Hybrid Permanent
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Senior Project Specialist, Clinical Supplies

This role involves coordinating clinical supply operations for Moderna’s mRNA-based therapeutics, ensuring investigational products are labeled, packaged, and distributed efficiently to clinical sites. The specialist will work cross-functionally with vendors and internal teams to maintain supply chain compliance, support IRT systems, manage temperature excursions, and drive digital innovation in supply operations.

Moderna Oxford, United Kingdom
Hybrid Permanent
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Audit Lead

Lead GMP/GDP audit strategy and execution for a key technology area such as sterile biologics or medical devices across Pfizer’s global manufacturing and supply network. Conduct complex audits at internal sites and external partners, assess compliance with global regulations, coach auditors, and drive continuous improvement in quality systems. Work cross-functionally to align audit practices with emerging regulatory trends and support inspection readiness.

Pfizer London, SW7 2AP, United Kingdom US$162,900 – US$271,500 pa
On-site Permanent
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Audit Lead

Lead GMP/GDP audit strategy and execution for a key technology area such as sterile biologics or medical devices within Pfizer’s global manufacturing and supply network. Conduct complex audits at Pfizer sites and external partners, ensuring compliance with global regulations and driving continuous improvement in quality systems. Provide expert coaching to auditors and collaborate across functions to address risks and enhance audit practices.

Pfizer US$162,900 – US$271,500 pa
On-site Permanent

Technical Service Engineer

This role involves providing on-site and remote technical support for advanced robotics solutions used in pharmaceutical and biotechnology environments. The engineer will perform diagnostics, preventative maintenance, and customer training, while acting as a key technical liaison between clients and internal teams. Responsibilities include managing service calls, spare parts forecasting, and using D365 for reporting, with a strong focus on customer satisfaction and problem resolution.

Wallace Hind Selection Sk138Ap, United Kingdom £52,000 – £56,000 pa
On-site Permanent
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Clinical Development Medical Director - Cardiovascular

This role involves leading clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and collaborate across functions to advance translational and clinical studies. The position emphasizes scientific leadership, regulatory engagement, and strategic input to bring innovative medicines to patients.

GSK
Hybrid Permanent
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Director Medical Writing Asset Lead

Lead medical writing strategy for one or more assets, primarily in Hepatology, across clinical development stages. Design and deliver high-quality clinical documents for global regulatory submissions, lead cross-functional teams, and drive process improvements using innovative technologies. This role involves shaping submission plans, mentoring teams, and influencing regulatory outcomes in a matrix environment.

GSK United Kingdom £119,250 – £198,750 pa
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Director Medical Writing Asset Lead

Lead the medical writing strategy for one or more pharmaceutical assets, primarily in Hepatology, ensuring high-quality clinical documents for global regulatory submissions. Drive process improvements, mentor teams, and lead complex submission projects in a matrix environment. This role involves shaping document strategy, managing cross-functional collaboration, and applying regulatory expertise across the drug development lifecycle.

GSK €119,250 – €198,750 pa
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Medical Director Clinical Development- Respiratory

This role involves leading clinical development for respiratory assets within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and deliver clinical and translational strategies, oversee study execution, ensure patient safety, and contribute to regulatory submissions. Working cross-functionally, they will help shape development plans that align with scientific innovation and patient needs, particularly in pulmonary hypertension and related areas.

GSK £222,750 – £371,250 pa
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(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

This role involves operating and monitoring advanced production equipment for mRNA vaccine manufacturing, ensuring compliance with cGMP and safety standards. The Manufacturing Associate will maintain accurate documentation, perform routine equipment maintenance, troubleshoot issues, and support continuous improvement initiatives within a highly regulated, digitized environment. Close collaboration with QA and cross-functional teams is essential to meet production KPIs and uphold process integrity.

On-site Temporary Clearance Required
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(Fixed-Term) Manufacturing Associate II - Shift Position

This role involves operating production equipment for mRNA vaccines in compliance with cGMP and safety regulations, performing routine maintenance, troubleshooting technical issues, and supporting continuous improvement initiatives within a 24/7 manufacturing environment. The candidate will work on the manufacturing floor at Moderna’s Harwell site, contributing to the production of safe and effective vaccines using cutting-edge mRNA technology. Emphasis is placed on digital proficiency, attention to detail, and active participation in a dynamic, cross-functional team.

On-site
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Facilities Engineering Manager

This role involves providing technical leadership for facility and utility systems at Moderna’s biotech manufacturing site in Harwell. The Facilities Engineering Manager ensures operational reliability, oversees vendor performance, and drives maintenance excellence across R&D and manufacturing environments. The position emphasizes continuous improvement, compliance, and the use of digital tools including AI-enabled systems, within a GMP-regulated setting.

On-site Permanent
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Sr Director and Team Lead, Regulatory Labelling Strategy and Development, Oncology

Leads a global team responsible for developing and managing regulatory labelling strategies for oncology products across the drug development lifecycle. Ensures compliance with global regulations, collaborates with cross-functional stakeholders in R&D, safety, and commercial teams, and engages with regulatory authorities to shape innovative, patient-focused labelling. Plays a strategic role in governance and policy development within GSK’s oncology portfolio.

GSK £221,925 – £369,875 pa