Latest Environmental Risk Assessment Scientist Jobs

GSK logo

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa
Hybrid Permanent
GSK logo

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex international environments.

GSK £144,375 – £240,625 pa
Hybrid Permanent

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis
On-site Permanent
AstraZeneca logo

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership, optimize investment decisions, and collaborate across functions to deliver high-impact strategic outcomes.

AstraZeneca United States
On-site Permanent
AstraZeneca logo

Executive Director, Strategy, Oncology R&D

This role involves crafting and driving the global Oncology R&D strategy, integrating clinical, scientific, and commercial insights to shape portfolio priorities. You will advise senior leadership on complex strategic topics, optimize investment decisions, and collaborate across functions to deliver impactful patient outcomes.

On-site Permanent

Clinical Data Analytics Lead

As Clinical Data Analytics Lead, you will transform complex clinical trial data into actionable insights, enhancing decision-making and data quality. You will collaborate with cross-functional teams to drive risk-based approaches, improve study oversight, and support patient outcomes using advanced analytics and visualization tools.

Novartis London, United Kingdom
Hybrid Permanent
Pfizer logo

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity 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 external committees and site-facing colleagues, to ensure the successful execution of clinical studies.

Pfizer
On-site Permanent
Pfizer logo

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity 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 supporting site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer
On-site Permanent
Moderna logo

(Fixed Term) Analyst, Quality Control, Chemistry & Stability

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
Moderna logo

(Fixed Term) Analyst, Quality Control, Chemistry & Stability

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 Gargrave, BD23 3RZ, 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 environments. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers.

Universal Business Team Taunton, Somerset, TA1 1HP, United Kingdom £35,000 – £40,000 pa
On-site Permanent

Mobile Service Technician - Medical Device Maintenance

This role involves maintaining and repairing advanced bio-decontamination and infection control equipment in healthcare and laboratory settings. Responsibilities include preventative maintenance, fault diagnosis, calibration, and providing technical training to customers. The technician will work on-site across South Wales and the South West of England, using ultrasonic vaporisation, hydrogen peroxide delivery, and embedded control systems.

Universal Business Team Weston-super-Mare, Somerset, United Kingdom £35,000 – £40,000 pa
On-site Permanent

Support technician

This role involves building, installing, and maintaining advanced electromechanical instruments across the UK, with significant time spent on customer sites. The technician will troubleshoot and repair equipment, support manufacturing processes, and contribute to product improvements through direct feedback to R&D. It combines field service, hands-on technical work, and collaboration across teams in a regulated environment.

Matchtech Whiteley, Hampshire, PO15 7LW, United Kingdom £30,000 – £35,000 pa
Hybrid Permanent

Quality Manager

This role involves leading and improving the ISO 13485 Quality Management System within a medical device manufacturer producing Class IIa and IIb products. The Quality Manager will manage non-conformances, CAPAs, and returned product investigations while supporting supplier quality and leading internal and external audits. The position operates in a hands-on manufacturing environment with a focus on regulatory compliance and continuous quality improvement.

ProTech Recruitment Ltd Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £60,000 – £70,000 pa
On-site Permanent

Microfluidics Engineer

SRG are delighted to be working with an innovative diagnostics organistion based in Scotland's Central belt as they look for a microfluidics engineer to support their product development function.The RoleAs Microfluidics Engineer you will be responsible for the design and...

SRG Coatbridge, Lanarkshire, ML5 3EH, United Kingdom £38,000 – £45,000 pa