Latest regulatory affairs Jobs

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and contributing to process improvements.

GSK

Hybrid Permanent

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and support inspections and quality events. The position offers opportunities for growth through complex regulatory work and direct impact on patient health.

GSK

Hybrid 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

Director Biostatistics - Hematology

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...

CSL

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Senior Scientist New Modalities, Analytical

This role involves defining and delivering analytical strategies for new modality medicines, such as peptides and oligonucleotides, from early development to commercial launch. You will work closely with cross-functional teams to ensure robust quality control, regulatory compliance, and efficient commercial supply, while leveraging digital tools and AI to enhance decision-making and process robustness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Quality Engineer

The Quality Engineer will manage and coordinate customer complaints for medical instruments and orthopaedic products, conduct internal audits, and maintain quality procedures. The role involves working independently, leading meetings, and ensuring regulatory compliance in a growing SME.

E-Personnel Recruitment Guildford, Surrey, United Kingdom £45,000 – £50,000 pa

Hybrid Permanent

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph

On-site Contract

Vulnerability Analyst

This role involves assessing known software vulnerabilities in Windows-based applications used in regulated medical devices. Responsibilities include performing exploitability and risk analysis, evaluating third-party component risks, and producing clear security documentation. The position requires 2+ years of commercial experience in application security and a strong understanding of CVEs and secure software concepts.

Real Limerick, Limerick County, Ireland £47 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

QA Officer, Pharmaceutical

The QA Officer will work in a biotech company, focusing on generating and reviewing SOPs, handling customer complaints, and maintaining GMP compliance. They will also participate in quality improvement initiatives, manage documentation, and support regulatory audits.

NMS Recruit Ltd t/a Russell Taylor Group Alderley Edge, Cheshire, SK10 4UB, United Kingdom £28,000 – £34,000 pa

Systems Engineer - Embedded and Hardware

This senior role involves leading the electronics and software workstream for IVD medical devices, ensuring robust system architecture, supplier governance, and regulatory compliance. The Systems Engineer will work closely with in-house teams and international suppliers, shaping architecture, design controls, and verification strategies.

Swiss Precision Diagnostics GmbH Cardington, Bedfordshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent

Head of Product Development & Engineering

This role involves leading the product development and engineering lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, mentoring a specialist team, and collaborating with quality, operations, and commercial teams to ensure regulatory compliance and commercial success.

Concept Technical Worthing, West Sussex, United Kingdom £70,000 – £80,000 pa

On-site Permanent