Latest Environmental Risk Assessment Scientist Jobs

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Senior Strategy Director (Senior Consultant) – Clinical Development – Evinova

This role involves leading the development and implementation of AI and digital health strategies to transform clinical development processes. The Senior Strategy Director will act as a trusted advisor, designing digital solutions for patient recruitment, remote monitoring, and data collection while driving innovation through AI. They will lead cross-functional teams, shape operating models, and ensure digital tools are integrated into clinical protocols with a focus on measurable value and patient outcomes.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Global Labelling Associate Director, Content

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 (Oncology)

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

Novartis

Hybrid Permanent

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 strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK Stevenage, United Kingdom

Hybrid Permanent

Deviation Owner

This role involves leading the investigation and resolution of manufacturing deviations in a GMP-regulated environment, ensuring compliance and product quality. The Deviation Owner will coordinate root cause analyses, drive corrective actions, and work across quality, production, and engineering teams to prevent recurrence. Emphasis is placed on data-driven problem solving, governance of deviation processes, and continuous improvement through structured methodologies like DMA/IC.

GSK Barnard Castle, United Kingdom

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions and high-quality medical execution across regions. The position requires deep oncology clinical and scientific expertise, strategic leadership, and collaboration with various stakeholders to deliver impactful medical outcomes globally.

Pfizer

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven medical impact. Responsibilities include leading the scientific narrative, data interpretation, and communication across regions, as well as engaging with clinical and research leaders to drive strategic decisions and continuous improvement.

Pfizer

On-site Permanent

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve data discrepancies and maintain inspection readiness.

Moderna Oxford, United Kingdom

On-site Temporary

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

The Data QC Specialist will perform detailed quality control reviews of laboratory data and documentation to ensure accuracy, traceability, and compliance with regulatory standards. This role involves working closely with laboratory scientists and data management teams to resolve discrepancies and maintain inspection readiness.

Moderna

On-site Temporary

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Senior Group Director, Safety Development & Processes

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive...

Roche Welwyn Hatfield, United Kingdom

Buyer - Pharmaceuticals

This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.

Cranleigh Scientific Ditton, Kent, ME20 6AE, United Kingdom £22,800 – £28,800 pa

Hybrid Flexible

Technical Documentation and Development Engineer

This role involves creating, managing, and improving technical documentation and CAD models for medical devices, ensuring compliance with MDR regulations. The engineer will own technical files, support product development and legacy improvements, and collaborate with R&D, regulatory, and manufacturing teams. Emphasis is placed on accuracy, regulatory adherence, and structured design control processes.

Michael Page Sheffield, South Yorkshire, United Kingdom £42,000 pa

On-site Permanent