Latest Environmental Risk Assessment Scientist Jobs

SERM Scientific Director

The SERM Scientific Director will lead the safety evaluation and risk management of GSK's key assets, ensuring scientifically sound review and interpretation of data. They will develop and execute safety strategies, manage safety governance, and represent GSK on cross-functional teams to address product safety issues and improve regulatory adherence.

GSK

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Research Scientist - Biologics Engineering - Protein Engineering and Novel Modalities - Novel Modalities R&I

This role involves designing and characterising innovative biologics, particularly multivalent and multi-specific formats and inhaled delivery. You will lead in silico design, integrate wet-lab data, and collaborate with ML scientists and experimentalists to translate digital concepts into validated molecules, accelerating the discovery pipeline.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Director Clinical Operations, Program Management

This role leads global clinical program delivery within AstraZeneca’s Oncology portfolio, focusing on strategic planning, operational excellence, and cross-functional leadership across late-stage development. The Executive Director will manage senior program directors, drive standardization, resolve escalated issues, and strengthen internal and external partnerships to accelerate patient impact. It involves governance, resource planning, financial stewardship, and leading organizational change in a dynamic, science-driven environment.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Associate Director, Regulatory Diagnostics

Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.

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

Hybrid 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 shaping labelling content, ensuring regulatory compliance, and collaborating with cross-functional teams to support successful product submissions and patient safety.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and support for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including investigators, regulatory bodies, and safety review teams.

Pfizer

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer will be responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer United Kingdom

On-site Permanent

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna Oxford, United Kingdom

On-site Contract

Senior Manager - Engineering & Maintenance

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.Moderna is establishing a leading research, development, and manufacturing facility at...

Moderna Oxford, United Kingdom

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing advanced bio-decontamination and infection control equipment in healthcare, pharmaceutical, and cleanroom settings. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Stroud, Gloucestershire, United Kingdom £35,000 – £40,000 pa

On-site Permanent

Electrical Field Service Engineer

Futures are working with a leading manufacture of medical devices in their search for an Electrical Field Service Engineer. You will offer support customers across the South of England, carrying out installation, commissioning, maintenance, and fault-finding activities on specialist electrical...

Permanent Futures Limited Coventry, West Midlands (county), United Kingdom £40,000 – £45,000 pa

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing specialist bio-decontamination and infection control equipment in healthcare, pharmaceutical, and cleanroom environments. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Cheltenham, Gloucestershire, United Kingdom £35,000 – £40,000 pa

On-site Permanent

Assembly Technician

This role involves assembling medical devices with precision and attention to detail, following detailed work instructions and maintaining accurate records. The technician will also support product development, testing, and continuous improvement activities in a regulated environment.

Euro Projects Recruitment Abingdon, Oxfordshire, OX14 5BH, United Kingdom £26,000 – £28,000 pa

On-site Permanent

Medical Devices Project Leader - Warwick

Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Provide technical leadership, mentor junior engineers, and ensure robust design and compliance, particularly for products involving injection-moulded plastic components. Contribute to regulatory strategy and full lifecycle development in a fast-paced environment focused on improving patient outcomes.

Newton Colmore Warwick, United Kingdom

On-site Permanent