Latest Environmental Risk Assessment Scientist Jobs

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, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Global Study Lead to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK Stevenage, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Director, Content

The Global Labelling Director, Content will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include shaping labelling content, maintaining core documents, and collaborating with cross-functional teams to ensure regulatory compliance and successful product submissions.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Head of Make CoE

The Head of Make CoE will lead the transformation of end-to-end manufacturing processes across a global network, partnering with sites and central teams to deliver safer, higher-quality, more sustainable, and more productive operations. Key responsibilities include strategy and roadmap leadership, governance, cross-functional integration, and team development, with a focus on digital and autonomous manufacturing.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

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

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, innovative thinking, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, 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, focusing on 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

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

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 Bristol, Bristol (county), United Kingdom £35,000 – £40,000 pa

On-site Permanent

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph

On-site Contract

Bank Physiotherapist - Women's Health

Bank Specialist Physiotherapist| Women's Health | Competitive Hourly Rate | Flexible Working | Fylde CoastWe have an exciting opportunity for an experienced Specialist Physiotherapist in Women's Health to join our bank staffing to support the Physio department on a flexible...

Spire Healthcare Blackpool, Lancashire, United Kingdom £19 – £24 ph

Scientist I, Molecular and Cell Biology

This role involves conducting cutting-edge research in molecular and cell biology, focusing on cell health and rejuvenation. Responsibilities include designing and executing experiments, developing new assays, and collaborating with multidisciplinary teams to advance translational projects and validate therapeutic targets.

Altos Labs Cambridge, United Kingdom £51,500 – £67,700 pa

On-site Permanent

Production Scheduler

This role involves planning, coordinating, and monitoring production activities across multiple projects in a regulated medical device manufacturing environment. You will work closely with manufacturing, engineering, quality, and supply chain teams to ensure delivery targets are met and continuously improve planning processes.

Euro Projects Recruitment Abingdon, Oxfordshire, OX14 5BH, United Kingdom £40,000 – £45,000 pa

On-site Permanent