Biotechnology Jobs

Trial Vendor Associate Director

This role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure vendor service excellence throughout the trial lifecycle.

Novartis United Kingdom

Remote Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director is responsible for developing and implementing strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They lead medical-scientific input, evidence generation, and stakeholder engagement to maximize the value of new medicines and support global medical affairs initiatives.

Novartis

Hybrid Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered on schedule, within budget, and to quality standards. You will collaborate closely with the Clinical Trial Team and vendor start-up managers, overseeing vendor interfaces, cost control, and service excellence.

Novartis United Kingdom

Hybrid Permanent Flexible

AI Acceleration Lead

This role focuses on driving AI innovation in clinical development by identifying operational bottlenecks, designing and running AI pilots, and translating findings into scalable solutions. The person will work across clinical operations, technology teams, and vendors to validate AI tools, generate evidence of value, and guide investment decisions. Emphasis is placed on hands-on testing, change management, and enterprise-wide adoption of AI-native capabilities.

GSK Stevenage, United Kingdom

On-site Permanent

DMPK Lead, London

As a DMPK Lead, you will drive the DMPK strategy for drug discovery projects, integrating quantitative pharmacology and AI-first approaches. You will design and implement DMPK strategies, optimize the use of datasets, and collaborate with interdisciplinary teams to advance drug design and development.

Isomorphic Labs United Kingdom

Hybrid Permanent

(Fixed Term) Warehouse Specialist

This role involves operating in a 24/7 GMP environment at Moderna’s UK manufacturing facility, ensuring seamless warehouse and logistics support. Responsibilities include managing inventory, verifying deliveries, coordinating shipments, and maintaining compliance with safety and operational standards.

Moderna

On-site Contract Shift-work

Team / Research Leader (Translational Oncology), London

This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.

Isomorphic Labs United Kingdom

Hybrid Permanent

Field Service Representative (Hampshire/Dorset area)

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche United Kingdom

Senior NPI Quality Engineer

Senior NPI Quality EngineerElectronics & Medical DevicesCompetitive Salary plus Bonus & BenefitsRelocation Assistance Provided (If Required)Step into a pivotal leadership role as a Senior NPI Quality Engineer and help bring high-quality, regulated products to life from first design through to...

Jonathan Lee Recruitment Jersey Marine, West Glamorgan, SA10 6JJ, United Kingdom

Pharmaceutical Manufacturing Manager

Leads pharmaceutical production operations, ensuring safety, quality, and regulatory compliance while driving continuous improvement through Lean Manufacturing. Oversees large manufacturing teams and collaborates with cross-functional departments to enhance site-wide performance. Focuses on operational excellence and strategic development within a regulated GMP environment.

Entrust Resource Solutions Devon, United Kingdom

On-site Permanent

Quality Assurance Specialist

This role involves maintaining and improving a Quality Management System in a medical device manufacturing environment, with a focus on regulatory compliance, documentation control, and audit management. The specialist will handle technical documentation, customer complaints, non-conformities, and CAPA activities while ensuring adherence to ISO13485 and EU MDR/IVDR standards. Close collaboration with senior management and external consultants is required to drive continuous quality improvements.

East Lancashire Services Manchester, United Kingdom

Hybrid Permanent

Capital Project Engineering Manager - Pharmaceuticals

Lead and deliver capital engineering projects in a GMP-regulated pharmaceutical environment, from concept to commissioning and handover. Oversee multidisciplinary teams, manage CAPEX budgets, and ensure compliance with regulatory and safety standards. Drive innovation and continuous improvement in engineering solutions while supporting long-term site development strategies.

Smart4Sciences North Yorkshire, United Kingdom

On-site Permanent

Quality Professional

This role involves maintaining and improving the Quality Management System for medical devices, ensuring compliance with ISO 13485 and FDA regulations. The professional will lead non-conformance investigations, manage CAPA processes, conduct risk assessments per ISO 14971, and support process validation and supplier quality activities. Close collaboration with R&D, manufacturing, and regulatory teams ensures quality is embedded across the product lifecycle.

Omega Resource Group Middleyard, Gloucestershire, United Kingdom

On-site Permanent

Project Quality Lead

This role involves leading quality strategy across the full product lifecycle in a pharmaceutical development environment. You'll drive design reviews, risk management, and quality system implementation while working closely with project teams and stakeholders. The position emphasizes proactive quality integration rather than post-hoc review, with a focus on influencing technical decisions and ensuring compliance through GMP and ISO standards.

Next Phase Recruitment United Kingdom

On-site Contract

Clinical & Validation Principal

Lead bioanalytical method development and validation activities within a GxP-regulated laboratory, overseeing HPLC, UPLC, and LC-MS/MS platforms. Manage a technical team, ensure regulatory compliance, and support audits and submissions. Focus on method optimisation, troubleshooting, and continuous improvement in a highly controlled environment.

Next Phase Recruitment Armagh, County Armagh, United Kingdom

On-site Permanent