Latest regulatory affairs Jobs

(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

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

Technical Manager – Polymer Materials

This role involves leading all polymer R&D activities, overseeing quality systems, and providing technical direction across manufacturing and regulatory activities. The Technical Manager will collaborate with senior management to drive innovation, ensure compliance, and support the transfer of new materials into production.

Talent STEM Ltd Hertford, United Kingdom £50,000 – £70,000 pa

On-site Permanent

Enterprise Trade Compliance Manager EMEA

Enterprise Trade Compliance Manager EMEAAs theEnterprise Manager for EMEA within Global Trade Compliance Team, you will play a pivotal role in driving the execution and continuous enhancement of CSL’s world-class import and export compliance program across the EMEA region.Your responsibilities...

CSL United Kingdom

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

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

Director, Medical Evaluation & Case Processing Oversight

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Director, Medical Evaluation & Case Processing Oversight

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Senior Project Manager, R&D: Drug Development

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Manager, Supply Chain Lead (SCL)

As a Manager, Supply Chain Lead, (SCL) your advanced knowledge and solid understanding of clinical study design and drug supply processes, you will lead and manage matrix teams responsible for the end to end oversight of supply chain activities required...

Pfizer Sandwich, United Kingdom

Document Manager, Pharmaceuticals

Document Manager - CAPEX Projects (Pharmaceutical Industry) Contract, Outside IR35We are seeking an experienced and detail-oriented Document Manager to support CAPEX (Capital Expenditure) projects within a dynamic pharmaceutical environment. This role is critical in ensuring the effective control, organization, and...

Smart4Sciences Crewe, Cheshire, United Kingdom

Contract

(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

Audit Lead

The Audit Lead role involves designing and maintaining audit strategies for key technology areas like sterile biologics, medical devices, and digital health. Responsibilities include leading audits, coaching auditors, partnering with cross-functional teams, and ensuring compliance with regulatory standards. The role focuses on continuous improvement, risk management, and innovation in Pfizer's quality management system.

Pfizer London, SW7 2AP, United Kingdom £50,000 – £70,000 pa

Remote Permanent

Senior Design Engineer – MedTech

Contract Design Engineer – MedTech (Outside IR35)ARCA is supporting an innovative MedTech organisation developing next-generation medical devices, looking to bring in an experienced Senior Design Engineer to support a key development phase.This is a hands-on role across the full product...

Arca Resourcing London, United Kingdom £50 – £55 ph

Senior Scientist

This role involves hands-on laboratory work, prototype development, and analytical method design for next-generation medical devices. You will work closely with multidisciplinary teams, including R&D, Quality, Regulatory, and Commercial functions, to innovate and develop cutting-edge products.

L-ev8 Recruitment Ltd Plymouth, Devon, United Kingdom £40,000 – £48,000 pa

On-site Permanent