Latest regulatory affairs Jobs

Quality Engineer (Compliance)

This role involves ensuring medical device and drug-device combination products meet strict regulatory standards throughout development. The Quality Engineer (Compliance) will lead design controls, risk management, and audit readiness activities, working closely with development teams and external partners. Key focus areas include DHF and RMF maintenance, regulatory compliance, and supporting clinical trial investigations.

Next Phase Recruitment Cambridge, Cambridgeshire, United Kingdom

Hybrid Contract

Quality Engineer

This role involves managing quality systems and asset calibration processes within a regulated medical devices environment. The Quality Engineer will oversee compliance with safety standards, maintain documentation integrity, and support audits while ensuring equipment is properly maintained. Training team members and improving health and safety performance are also key responsibilities.

Randstad Delivery Witney, Oxfordshire, United Kingdom £57,000 pa

On-site Contract

DMPK Lead, London

As a DMPK Lead, you will drive the DMPK strategy for drug discovery projects, integrating quantitative pharmacology and AI-first approaches. You will design and implement DMPK strategies, optimize the use of datasets, and collaborate with interdisciplinary teams to advance drug design and development.

Isomorphic Labs United Kingdom

Hybrid Permanent

Team / Research Leader (Translational Oncology), London

This role involves leading the development and execution of comprehensive translational strategies for Isomorphic Labs' oncology pipeline. You will collaborate with interdisciplinary teams, manage a group of biologists, and ensure the successful transition of AI-designed drugs from preclinical to clinical stages.

Isomorphic Labs United Kingdom

Hybrid Permanent

Global Supply Chain Analyst

This role involves optimising global supply chain operations for a medical devices company by managing inventory, supporting supply/demand planning, and delivering data-driven insights. The analyst will work closely with international teams to resolve logistical challenges, ensure regulatory compliance, and drive process improvements within a highly regulated environment. Key focus areas include backorder management, new product introductions, and maintaining audit-ready documentation.

Randstad Delivery Witney, Oxfordshire, United Kingdom £47,000 pa

On-site Contract

Senior Scientist 2 MSAT

This role involves leading the transfer and scale-up of bioprocesses from development into GMP manufacturing environments. The scientist will design and oversee technical studies, ensure regulatory compliance, and support root cause analysis and process robustness. Working closely with cross-functional teams, they will drive successful process implementation in a highly collaborative, multidisciplinary setting.

SRG Darlington, County Durham, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.

Moderna Oxford, United Kingdom

On-site Permanent

Associate Engineer, GxP IT Support

This role involves supporting Moderna’s manufacturing operations at the Harwell site, ensuring GMP compliance and providing Tier 1 IT support. Responsibilities include maintaining robust IT systems, triaging incidents, managing infrastructure, and collaborating with various teams to ensure smooth operations. The position offers exposure to modern cybersecurity and automation tools, making it a dynamic and challenging opportunity in the biotech industry.

Moderna

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

SERM Associate Medical Director

This role involves providing medical and scientific expertise in safety evaluation and risk management for GSK's clinical and post-marketing assets. Responsibilities include signal detection, data analysis, and communication of safety risks, as well as supporting safety governance and cross-functional teams.

GSK United Kingdom

Hybrid Permanent

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role involves leading the quality oversight of external partners in R&D and regulated activities, managing the vendor lifecycle from due diligence to continuous improvement, and ensuring compliance with GLP/GCP/GMP/GVP standards. The position requires close collaboration with various departments to maintain high-quality standards and regulatory compliance.

CSL United Kingdom

On-site Permanent

GMP Vendor Oversight and QA Lead

This role involves leading the quality oversight of external partners in R&D and regulated activities, ensuring compliance with GxP standards. Responsibilities include vendor lifecycle management, risk-based monitoring, quality agreements, and cross-functional collaboration to maintain high-quality standards and continuous improvement.

CSL United Kingdom

On-site Permanent

Director, Immunotoxicology, Immune Safety

This role involves leading the immunotoxicology strategy across AstraZeneca's BioPharma and Oncology portfolios, guiding the design and execution of experimental strategies to assess and mitigate immune-related toxicities. You will collaborate with multidisciplinary teams, influence project direction, and build a high-performing team in a highly collaborative and innovative environment.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

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

Director, Oncology Business Planning Lead

Currently looking to identify aDirector Business Planning to join the Business Planning Operations and Transformation (BPOT) team. They have a pivotal role within the Global Oncology and Hematology Business Unit (OBU) in helping to achieve our bold ambition of eliminating...

AstraZeneca Cambridge, United Kingdom