Latest Innovation Jobs

Fluidic System Engineer - Pathogen

Design and develop microfluidic systems for a point-of-care diagnostic device that enables metagenomic sequencing through a cartridge-based interface. Work closely with cross-functional teams to integrate microfluidics with instrumentation, electronics, and firmware, focusing on robustness, automation compatibility, and real-world performance. Conduct prototyping, testing, and validation using techniques like soft lithography and rapid prototyping to advance decentralized infectious disease diagnostics.

Ellison Institute of Technology Oxford, United Kingdom

On-site

Postdoctoral Research Fellow - Generative Biology Institute

Conduct independent, high-impact research in a multidisciplinary environment focused on engineering biology, with responsibilities including experimental design, data analysis, publication, and mentoring junior researchers. Work at the intersection of biology, technology, and engineering within a newly established, well-resourced institute pursuing transformative solutions in health, agriculture, and sustainability.

Ellison Institute of Technology Oxford, United Kingdom £40,000 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for internal medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapeutics. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £214,900 – £358,100 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, with accountability for designing and executing global clinical development plans. The individual will guide cross-functional teams through trial design, regulatory submissions, and lifecycle management, while serving as a therapeutic expert and strategic partner across internal and external stakeholders. Emphasis is placed on innovation, patient engagement, and compliance with global regulatory standards.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Install, service, and repair advanced medical diagnostic systems in NHS and private pathology laboratories. Perform breakdown maintenance, calibration, and technical support for complex laboratory equipment on customer sites. Work with cutting-edge diagnostic technologies in a customer-facing field role requiring strong technical and interpersonal skills.

TRS Consulting Newport, Gloucestershire, Gloucestershire, GL13 9PY, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

This role involves installing, servicing, repairing, and calibrating advanced medical diagnostic systems in NHS and clinical laboratories. The engineer will work on complex laboratory equipment, including flow cytometry and cell separation devices, providing technical support directly at customer sites. The position requires strong field service skills in electro-mechanical systems and a commitment to high-level customer service in sensitive healthcare environments.

TRS Consulting Bath, Somerset, United Kingdom £52,000 pa

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.

GSK US$169,950 – US$283,250 pa

On-site Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will oversee safety governance, lead cross-functional teams, and ensure compliance with global regulations. They will analyze clinical data, manage safety issues, and contribute to regulatory submissions and long-term clinical strategy.

GSK US$169,950 – US$283,250 pa

On-site Permanent

Maintenance Engineering Manager - Packaging

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna’s Harwell site, from initial design through commissioning and validation. Establish maintenance strategies, ensure GMP compliance, and drive continuous improvement using engineering excellence principles and digital tools. Build and lead a high-performing engineering team to support long-term operational success in a regulated biotech environment.

Moderna

Hybrid Permanent

Sr. Manager, Site Budgets and Contracts

This role involves leading the creation and management of investigator site budgets and contracts for global clinical trials, using Grants Manager and FMV benchmarking tools. The Senior Manager collaborates with CROs, Legal, and Clinical Operations to ensure site budgets align with study forecasts and are executed on time. Responsibilities include strategic planning, contract negotiation oversight, risk identification, and process improvement within an outsourced trial model.

Moderna

Hybrid Permanent

Director, Biostatistics

This role involves leading statistical strategy for gene therapy clinical development programs, with responsibilities spanning study design, regulatory engagement, and analysis oversight. The Director will ensure scientific and regulatory rigor in clinical trials, manage vendor performance, and contribute to submissions and publications. It is a hands-on leadership position within a cross-functional team environment.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

Health, Safety and Compliance Specialist

This role involves leading health, safety, and biological compliance across a gene therapy organisation, with a focus on regulatory adherence, risk assessment, and biosafety oversight. The specialist acts as the appointed Biological Safety Officer, ensuring safe handling of biological materials and driving a strong safety culture through training and audits. Work includes developing safety systems, incident investigation, and maintaining compliance with UK legislation and internal standards.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

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Multi-Skilled Engineer II

The Multi-Skilled Engineer II role involves maintaining and repairing pharmaceutical equipment and facility installations to support manufacturing and QC operations. Responsibilities include diagnosing and repairing equipment, conducting risk assessments, planning maintenance, managing critical spares, and providing support to other teams.

Autolus Stevenage, United Kingdom

A

Associate Director, Operational Intelligence

This role focuses on building advanced operational models and simulations to optimise Autolus' end-to-end processes across manufacturing, testing, supply chain, and quality. The individual will integrate data from multiple systems to create analytical frameworks that drive strategic decisions, improve capacity planning, and support business cases. It is a highly technical, insight-driven position requiring deep expertise in data modelling, cross-functional collaboration, and problem-solving in a regulated biopharmaceutical environment.

Autolus Stevenage, United Kingdom

On-site Permanent

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions. Develops strategic regulatory input for safety reports, variations, and renewals, while acting as a liaison with health authorities. Supports global approval processes and contributes to process improvements and team mentorship.

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

Hybrid Permanent