Latest leader Jobs

Field Service Engineer, Medical Diagnostic Systems

Field Service Engineer, Medical Diagnostic SystemsBasic Salary Up To £50,000Overall Earnings £60,000+Bonus 15%£10 Per Day Lunch AllowanceCompany CarPensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Medical Diagnostic SystemsThis market leader seeks to recruit a technically motivated and customer focused Field...

TRS Consulting Swindon, Wiltshire, United Kingdom £50,000 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Field Service Engineer, Medical Diagnostic SystemsBasic Salary Up To £50,000Overall Earnings £60,000+Bonus 15%£10 Per Day Lunch AllowanceCompany CarPensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Medical Diagnostic SystemsThis market leader seeks to recruit a technically motivated and customer focused Field...

TRS Consulting Reading, Berkshire, United Kingdom £50,000 pa

On-site Permanent

Manager, Supply Chain Lead (SCL)

As a Manager, Supply Chain Lead, (SCL) your advanced knowledge and solid understanding of clinical study design and drug supply processes, you will lead and manage matrix teams responsible for the end to end oversight of supply chain activities required...

Pfizer Manchester, M1 4HD, United Kingdom

Manager, Supply Chain Lead (SCL)

As a Manager, Supply Chain Lead, (SCL) your advanced knowledge and solid understanding of clinical study design and drug supply processes, you will lead and manage matrix teams responsible for the end to end oversight of supply chain activities required...

Pfizer

Interventional Study Scientist Director

This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.

GSK United Kingdom

On-site Permanent

Specialist, R&D Contracts & Business Operations

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Sr. Manager, ICSR Quality

The Opportunity:Reporting to the Head of Risk Management, Aggregate Reports & Pharmacovigilance, as theSenior Manager, ICSR Quality, you will have Individual Case Safety Reports (ICSRs) accountability and you will be responsible for the oversight and control of the operational management...

CSL

Director / Senior Director, Precision Diagnostics - Oncology

This role involves leading the development and execution of precision diagnostics strategies for oncology programs, working cross-functionally with research, clinical, regulatory, and commercial teams. Responsibilities include defining diagnostic requirements, overseeing project plans, and engaging external partners to accelerate assay development and regulatory submissions.

GSK

(Fixed Term) Manufacturing Associate I

The Manufacturing Associate will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. Responsibilities include maintaining documentation, troubleshooting equipment, and participating in continuous improvement projects in a fast-paced, team-oriented environment.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

Qualified UK and European Patent Attorney - Cell engineering, immunology and immunotherapy 3 days a week, maternity cover 10 months

This role involves supporting Quell’s scientific and project teams in identifying and protecting IP, drafting and prosecuting patent applications, and monitoring third-party IP. The position is part-time, 3 days a week, for 10 months to cover maternity leave, and requires a strong background in cell and protein engineering, immunology, and immunotherapy.

Quell Therapeutics London, United Kingdom

On-site Temporary Part-time

Principal Scientist, TechBio Discovery

Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...

Recursion North Tyneside, NE29 8EP, United Kingdom US$198,000 – US$271,700 pa

Hybrid Permanent

Principal Scientist, TechBio Discovery

Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...

Recursion United Kingdom £198,000 – £271,700 pa

Hybrid Permanent

Director, Project Toxicologist – Oncology Targeted Delivery Safety Science

The Director, Project Toxicologist role involves leading the design and execution of regulatory and investigative toxicology studies for novel oncology therapies, including Radio Conjugates and Antibody Drug Conjugates (ADCs). You will collaborate with cross-functional teams to drive innovative safety strategies, inform candidate selection, and support regulatory submissions, contributing to the acceleration of transformative oncology treatments.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Regulatory Transparency (Disclosures) Professional

In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent