Latest Environmental Risk Assessment Scientist Jobs

GSK logo

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK
Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis London, United Kingdom
Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

This role involves developing and maintaining global labelling strategies and core documents for pharmaceutical products. You will lead cross-functional discussions, present labelling proposals, and ensure compliance with regulatory requirements across different markets.

Novartis
Hybrid Permanent
GSK logo

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
AstraZeneca logo

Automation/Process Control Engineer

This role involves strengthening control systems in AstraZeneca's manufacturing network, using digitalization and Lean techniques to improve production speed, resilience, and quality. The engineer will manage small projects, provide technical support, and mentor peers in automation and control systems.

AstraZeneca Macclesfield, United Kingdom
On-site Contract
AstraZeneca logo

Regulatory Affairs Manager

Regulatory Affairs ManagerType: PermanentLocation: Pancras Square, LondonIntroduction to roleDeliver and maintain competitive licences for the UK, driving regulatory strategy for new initiatives and ensuring regulatory compliance for defined product and project responsibilities, including project leadership. Achieve timely delivery of clinical...

AstraZeneca London, United Kingdom
Pfizer logo

Clinical Development Medical Director (Associate Director)

This role involves overseeing the 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 providing clinical support to the study team. The position also involves mentoring others and contributing to strategic discussions with key stakeholders.

Pfizer
On-site Permanent
Pfizer logo

Clinical Development Medical Director (Associate Director)

This role involves overseeing the 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
On-site Permanent

Lead Manufacturing Engineer - NPI

The Lead Manufacturing Engineer will take ownership of manufacturing development activities, from early concept through to prototype and low-volume production. You will help define manufacturing strategy, assembly processes, tooling, and automation solutions for first-generation products, working closely with design engineers and external suppliers.

Redline Group Headington, Oxfordshire, United Kingdom £60,000 – £70,000 pa
On-site Permanent
Autolus logo

Executive Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom
Hybrid Permanent
Autolus logo

Supply Planner

The Supply Planner ensures uninterrupted production by managing raw material procurement and inventory across clinical and commercial manufacturing operations. This role involves running MRP processes, maintaining inventory policies, coordinating with suppliers and 3PLs, and leading supply continuity efforts. The position works cross-functionally with finance, quality, and manufacturing teams to align supply plans with demand forecasts and resolve supply chain disruptions.

Autolus Stevenage, United Kingdom
Hybrid Permanent
Recursion logo

Research Synthesis Chemist

Your work will change lives. Including your own.The Impact You’ll MakeWe are growing our chemistry team at Recursion and are seeking a Research Synthetic Chemist to join our Automated Chemistry group. We are looking for an individual that thrives in...

Recursion Crathes, Alba / Scotland, United Kingdom

Locum Biomedical Scientist

The role involves performing complex molecular diagnostic tests and maintaining high-quality laboratory practices to support patient care. Responsibilities include sample preparation, analysis, and communication with healthcare professionals, while ensuring compliance with UKAS accreditation standards.

MSI Recruitment Fairlands, Surrey, GU3 3JH, United Kingdom £21 – £23 ph
On-site Temporary

Specialist Biomedical Scientist - Microbiology

Job Title: Specialist Biomedical Scientist - MicrobiologyLocation: BasildonSalary: £39,959 - £48,117 per annum + £10,000 Joining Bonus and wellbeing allowanceJob Type: Full Time, PermanentWe are expanding and are looking for an experienced Specialist Biomedical Scientist (BMS) who is ready to...

Synlab Basildon, Essex, United Kingdom £39,959 – £48,117 pa

Pharmaceutical Manufacturing Process Operator

The role involves setting up and operating manufacturing equipment in a highly regulated pharmaceutical environment, ensuring products meet quality standards and compliance with cGMP, health and safety, and company procedures. Responsibilities include accurate documentation, equipment maintenance, and supporting continuous improvement initiatives.

ARx Recruitment Services Watford, Hertfordshire, United Kingdom £28,000 pa
On-site Permanent