Latest Environmental Risk Assessment Scientist Jobs

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Senior Counsel

The Senior Counsel provides comprehensive legal support and advice to AstraZeneca's UK marketing company, focusing on AI, data privacy, and commercial matters. They will act as a subject matter expert, draft and review legal documents, and ensure compliance with regulations and internal policies.

AstraZeneca London, United Kingdom

On-site Permanent

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Statistics Leader / Associate Director – Oncology Statistics

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares...

GSK

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Scientific Programme Administrator, Clinical Genomics

The role involves supporting the delivery of high-quality genomics-based External Quality Assessment (EQA) schemes, working closely with scientific and operational teams to ensure accurate and reliable genetic test results. Responsibilities include sample preparation, data handling, quality management, and laboratory support, contributing to international standards in diagnostic genomics.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £32,442 pa

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The position also includes mentoring others and contributing to protocol design and study strategy.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer United States

On-site Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Mechanical Design Engineer

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at an exciting stage of its growth. Developing next generation wearable medical devices designed to deliver clinically meaningful physiological insights beyond the hospital environment, the business...

Cure Talent Loughborough, Leicestershire, LE11 2QG, United Kingdom £30,000 – £40,000 pa

QA/RA Assistant/Manager

This role involves supporting quality, regulatory, and information security processes in a growing laboratory setting. Responsibilities include maintaining the Integrated Management System, ensuring compliance with various standards, managing controlled documentation, and assisting with audits and risk management.

Guilford Street Laboratories Liverpool, Merseyside, United Kingdom £35,000 – £45,000 pa

On-site Permanent

Patient Safety Partner

The Patient Safety Partner will support individual case safety reports, assess pharmacovigilance requirements, and manage local safety risks within ophthalmology. They will also assist with global safety solutions, product launches, and cross-functional collaboration with Medical Affairs and Clinical Operations.

Talentmark Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £50 – £66 ph

Hybrid Contract

Supplier Quality Engineer

As a Supplier Quality Engineer, you will lead the supplier quality management programme, working closely with Engineering, Manufacturing, and Quality teams to ensure suppliers meet regulatory, technical, and quality requirements. You will conduct supplier audits, manage quality agreements, and support design reviews and risk management, all while ensuring compliance with ISO 13485 and FDA 21 CFR Part 820.

ProTech Recruitment Ltd Oxfordshire, United Kingdom £50,000 – £55,000 pa

Hybrid Permanent

Pharmaceutical Quality Engineer

The role involves providing quality engineering support across manufacturing, validation, and supply chain operations, ensuring compliance with GMP and GDP standards. Key responsibilities include leading deviation investigations, managing CAPA processes, and collaborating with cross-functional teams to drive continuous improvement in quality systems.

Smart4Sciences Cheshire, United Kingdom

On-site Contract Flexible