Latest Pharmaceuticals Jobs

Executive Director, Asset Project Leadership

Lead strategic execution of drug development programs across Recursion's portfolio, aligning cross-functional teams from preclinical to clinical stages. Leverage Recursion OS and ClinTech insights to drive data-driven decision-making, optimize project workflows, and accelerate delivery of transformative medicines. Foster a culture of innovation, accountability, and urgency to advance novel therapeutics through stage-gates with a focus on patient impact.

Recursion North Tyneside, NE29 8EP, United Kingdom US$297,000 – US$356,400 pa

Hybrid Permanent

Research Scientist, Immunology

This role involves designing and executing complex in vitro assays using primary human immune cells and patient-derived tissues to support drug discovery in immunology. The scientist will contribute to target validation, mechanism of action studies, and small molecule screening, leveraging advanced technologies like flow cytometry and high-content imaging. Working within cross-functional teams, they will integrate immunology expertise into both in vitro and in vivo workstreams across the therapeutic pipeline.

Recursion Crathes, Alba / Scotland, United Kingdom £52,000 – £70,400 pa

On-site 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

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site Permanent

Scientist – Peptide Chemistry

This role involves conducting laboratory-based experimental work in peptide chemistry, designing and synthesizing peptides using solid-phase techniques, and contributing to the development of new peptide medicines. The position offers opportunities for personal and professional growth within a dynamic and collaborative team.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Medical Information Specialist

This role involves providing high-quality medical information to healthcare professionals, developing digital content for HCP and patient websites, and generating insights to support brand strategies. You will work closely with cross-functional teams to ensure clear and compliant scientific communication, focusing on Respiratory, Immunology, and Vaccines.

AstraZeneca London, United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna Oxford, United Kingdom

Senior Manager - Engineering & Maintenance

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Director (Team Lead), Content

This role involves leading a team of labelling professionals, developing global labelling strategies, and ensuring compliance with regulatory requirements. The Director will collaborate with cross-functional partners and drive continuous improvement in labelling processes.

Novartis London, United Kingdom

Hybrid Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

ML Research Engineer, London

This role involves translating research concepts into practical AI implementations, optimizing models, and collaborating with scientists and engineers to advance drug discovery. You will work on state-of-the-art ML models, design experiments, and develop specialized tools to support the team's innovative projects.

Isomorphic Labs London, United Kingdom

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer Sandwich, United Kingdom

On-site Permanent

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence, and managing the delivery of clinical trial data and regulatory documents.

Pfizer Cambridge, United Kingdom

On-site Permanent

Head of Global Regulatory Affairs and Strategy

This senior leadership role involves defining and optimizing global regulatory strategies for drug development programs, building a regulatory team and systems, and implementing quality, pharmacovigilance, and medical writing frameworks. The role leverages AI to streamline regulatory workflows and ensure rapid global approval of products.

Isomorphic Labs Cambridge, United Kingdom

On-site Permanent