Latest Innovation Jobs

Senior SME - MSAT EM Tech Ops DS DP

This role involves leading technical operations and providing strategic support for the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, collaborating with external manufacturing partners, and ensuring compliance with GMP standards and continuous improvement initiatives.

GSK United States

On-site Permanent

Senior SME - MSAT EM Tech Ops DS DP

This role involves collaborating with internal and external stakeholders to support the commercial manufacture of large molecule drug substances and sterile drug products. Responsibilities include executing technical strategies, providing technical support, and ensuring compliance with GMP standards. The role also focuses on continuous improvement, change control, and managing critical lifecycle activities.

GSK

On-site Permanent

Senior Clinical Trial Manager

The Senior Clinical Trial Manager will manage the execution of clinical trials from start to closure, working closely with the Clinical Project Manager and cross-functional teams. Responsibilities include tracking trial activities, building relationships with CROs, and identifying process improvements. The role is crucial for advancing Recursion's drug development portfolio and ensuring operational excellence across clinical programs.

Recursion United Kingdom £136,200 – £192,200 pa

Hybrid Permanent

Senior Clinical Project Manager

The Senior Clinical Project Manager will lead the execution of one or more clinical trials from start to finish, ensuring compliance with regulations and managing cross-functional teams. This role involves planning, budgeting, and overseeing global clinical trials, with a focus on early phase oncology studies.

Recursion United Kingdom £165,900 – £211,100 pa

Hybrid Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. You will develop and implement AI/ML models, automate manual processes, and create decision-support tools to improve operational efficiency. The role requires strong expertise in machine learning, software engineering, and cloud deployment, with a focus on practical, scalable solutions.

Pfizer

On-site Permanent

Director, AI Engineering--Clinical Development and Operations (CD&O)

This role involves designing, building, and deploying production-grade AI systems to support clinical development and operations. Key responsibilities include developing AI/ML models, automating manual processes, creating predictive models, and implementing robust AI solutions in a cloud environment. The role requires strong collaboration with cross-disciplinary teams to ensure AI solutions are aligned with real scientific needs and are adopted in day-to-day operations.

Pfizer

On-site Permanent

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent

Global Program Clinical Head (Neuroscience)

As a Global Program Clinical Head, you will lead end-to-end clinical development programs in Neuroscience, driving strategy, execution, and regulatory compliance. You will collaborate with global teams, influence key decisions, and ensure patient-centric clinical trials.

Novartis London, United Kingdom

Downstream/Purification Senior Scientist

This role involves developing and optimizing downstream purification processes for biologics and advanced therapies. Responsibilities include designing and executing process development studies, supporting scale-up and technology transfer, and collaborating with cross-functional teams to deliver project objectives.

Walker Cole International Dublin, Alba / Scotland, IV17 0YF, United Kingdom €50,000 – €65,000 pa

On-site Permanent

Process Project Engineer – Moulding / Manufacturing

Process Project Engineer – Moulding / ManufacturingRoleExciting new role with our client a multinational Medical Device and Healthcare products provider. NIRAS is actively recruiting for an energetic and hands-on Manufacturing/Project Engineer to lead a key project within our Client’s Advanced...

NIRAS Ireland Castlebar, Mayo County, Ireland

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Laboratory Coordinator

As a Laboratory Support Coordinator, you will install and support advanced laboratory systems, provide customer training, troubleshoot technical issues, and offer sales support. You will work closely with a skilled team, contributing to exciting projects and making a difference in healthcare.

Adecco London, United Kingdom £200 – £230 pd

On-site Contract

Global Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States

On-site Permanent

Global Study Lead

The Global Study Lead is responsible for overseeing the design, planning, execution, and documentation of clinical studies, ensuring compliance with regulatory requirements and delivering high-quality results within budget and timelines. The role involves leading cross-functional teams, collaborating with internal and external stakeholders, and managing study-level budgets and operational aspects.

Roche

On-site Permanent