Latest Managed Services Jobs

CMC Project Lead (Next Generation Biologics and ADCs), London

Lead the CMC strategy for next-generation biologics and Antibody-Drug Conjugates (ADCs), driving end-to-end technical development from AI-designed candidates to clinical manufacturing. Orchestrate complex processes including cell line development, conjugation chemistry, analytical characterization, and regulatory filings, while managing global CDMO partnerships and ensuring compliance with cGMP and global regulatory standards.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Medicinal Drug Design Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Team Leader, Medicinal Drug Design, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom

Associate Director (Analytical Team Leader]), Early Chemical Development, Pharmaceutical Science

This role involves leading an analytical team in early chemical development, ensuring the delivery of high-quality analytical work to support GMP manufacturing and stability. The position requires extensive experience in analytical science, a passion for team development, and the ability to drive organizational effectiveness and innovation.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Automotive Electrical Engineer

Automotive Electrical Systems Engineer📍 Crewe, Cheshire (Hybrid Working) 🏢 Bentley Motors ⏱ 35 hours per week 📅 Contract until 31 December 2026Adecco in partnership with Bentley Motors is seeking an experienced Electrical Systems Engineer to support the development of innovative...

Adecco Crewe, Cheshire, United Kingdom

QA/ Validation Supervisor, Pharmaceutical

This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.

NMS Recruit Ltd t/a Russell Taylor Group Walkden, Manchester, M28 3DR, United Kingdom £40,000 – £45,000 pa

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

Global Development Lead, Early Clinical Development, Internal Medicine

The Global Development Lead will drive clinical research for cardiometabolic diseases, creating early clinical development strategies and leading the translation of pre-clinical observations into Phase 1/2 studies. They will work closely with cross-functional teams to ensure medical and scientific excellence, manage clinical trial execution, and engage with regulatory authorities and external collaborators.

Pfizer Sandwich, United Kingdom

On-site Permanent

Director, Development Unit CQA Program Lead

Salary Range:£78,400.00 - £145,600.00Job Description Summary#LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London (The Westworks), United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Shaping the future of clinical development requires...

Novartis London, United Kingdom

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. The candidate will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous improvement initiatives. It's a key position influencing patient access to medicines through robust lifecycle management.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Global Program Safety Team Lead - Neuroscience

This role involves leading medical safety strategy for neuroscience drug development programs at Novartis, managing global cross-functional teams, and ensuring robust benefit-risk evaluation throughout the product lifecycle. The position requires deep expertise in safety signal detection, regulatory submissions, and mentoring safety professionals, with a strong focus on clinical development and lifecycle management. Based in London or remotely, the role plays a key part in shaping global safety standards and driving patient-centric innovation.

Novartis London, United Kingdom £104,790 – £194,610 pa

Hybrid Permanent

Expert Scientific Writer

This role involves leading the development of scientific publications such as manuscripts, abstracts, posters, and presentations by transforming complex clinical data into clear, accurate, and impactful content. The Expert Scientific Writer will guide materials from concept to publication, ensuring alignment with scientific narratives and industry guidelines while collaborating with cross-functional teams. The position supports global medical affairs initiatives and emphasizes high-quality, evidence-based communication across therapeutic areas.

Novartis London, United Kingdom £46,550 – £86,450 pa

Hybrid Permanent

Associate Director, Statistical Programming

This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Pharmaceutical Regulatory Affairs Officer

This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.

Evolve Selection Leicester, Leicestershire, United Kingdom £40,000 – £50,000 pa

Hybrid

Associate Director, Global Publications & Foundational Content

Salary Range:£67,900.00 - £126,100.00Job Description SummaryAre you passionate about transforming complex scientific data into publications that shape healthcare and improve patient outcomes worldwide? As an Associate Director, Global Publications & Foundational Content, you will lead the development of high-impact scientific...

Novartis London, United Kingdom