Latest regulatory affairs Jobs

Global Regulatory Affairs Manager

Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across regions. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on strategic planning, regulatory intelligence, and process innovation within a patient-first framework.

GSK United Kingdom

Global Regulatory Affairs Manager

Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across markets. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on innovation, patient impact, and strategic alignment within a matrix environment.

GSK

Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves leading the development and maintenance of global labelling strategies and core documents for oncology products, ensuring scientific accuracy and regulatory compliance. The individual will facilitate cross-functional alignment, analyse regulatory and competitor data, and support health authority interactions. Based remotely or in London, the position plays a key part in shaping product information across global markets.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves leading the development and maintenance of global labelling strategies and core documents for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will work cross-functionally to align labelling content, interpret clinical data, and ensure compliance with global regulatory standards. Key responsibilities include supporting health authority interactions, mentoring team members, and maintaining scientific accuracy across product lifecycles.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Global Regulatory Science, CMC

Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.

Moderna London, United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety across the product lifecycle, focusing on clinical safety evaluation, signal detection, and risk management. Oversees production of key pharmacovigilance documents and ensures compliance with regulatory standards. Acts as safety representative in cross-functional teams and drives safety specifications and risk mitigation plans.

CSL

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL

Senior Medical Director Early Clinical Respiratory

This role involves leading early-phase clinical development in respiratory therapeutics, designing and overseeing Phase 1 and 2a trials, and translating scientific innovation into clinical proof-of-concept. The individual will act as a medical expert, shaping clinical strategies, guiding regulatory interactions, and mentoring teams within a global, collaborative environment. Emphasis is placed on biomarker use, translational research, and engagement with external scientific leaders.

AstraZeneca Cambridge, United Kingdom

Health, Safety and Compliance Specialist

This role involves leading health, safety, and biological compliance across a gene therapy organisation, with a focus on regulatory adherence, risk assessment, and biosafety oversight. The specialist acts as the appointed Biological Safety Officer, ensuring safe handling of biological materials and driving a strong safety culture through training and audits. Work includes developing safety systems, incident investigation, and maintaining compliance with UK legislation and internal standards.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

Electronic System Engineer

Electronic System EngineerNewcastle Upon Tyne, United KingdomSalary: CompetitiveJackson Hogg is delighted to be working with a leading diagnostics business which is scalng up it's engineering team due to new international investment. This is for a dynamic electronics engineer who can...

Jackson Hogg Newcastle upon Tyne, Tyne & Wear, NE1 4JA, United Kingdom £40,000 – £55,000 pa

Head of Quality - Pharmaceuticals

Leads quality assurance and control functions within a pharmaceutical manufacturing and import environment, ensuring compliance with EU GMP standards. Responsible for maintaining inspection-readiness, managing regulatory audits, and serving as the primary liaison with the MHRA. Develops and drives the site's Quality Management System as a member of the Site Leadership Team.

Smart4Sciences Manchester, United Kingdom £60,000 – £65,000 pa

Validation Technician (Graduate or Technical Entry Level)

This role involves executing and reporting validation protocols for critical equipment, facilities, and systems in a regulated manufacturing environment. The technician will conduct temperature mapping, air particle counting, airflow studies, and support sterilisation process revalidation. It offers hands-on technical work with comprehensive training, ideal for someone starting a career in quality and validation within life sciences or pharmaceuticals.

Cherry Professional South Wigston, Leicestershire, LE18 4TH, United Kingdom £30,000 – £33,000 pa

Microfluidics Engineer

Design and develop microfluidic sample preparation systems for a diagnostic platform that enables rapid bacterial identification and antimicrobial susceptibility testing from whole blood. Work across the full lifecycle from concept to scale-up, conducting prototyping, experimental validation with biological samples, and design for manufacturability within a regulated environment. Collaborate closely with scientists and engineers to optimise fluidic performance and ensure robust, scalable microfluidic cartridges.

Platform Recruitment Oxford, Oxfordshire, United Kingdom £50,000 – £75,000 pa

Senior Scientist - Assay Development

Lead the development and optimisation of quantitative immunoassays for at-home diagnostic tests, from concept through validation and commercialisation. This hands-on role involves designing and executing studies, ensuring regulatory compliance, and managing external collaborators. Work with human biological samples and translate lab-based assays into point-of-care formats such as lateral flow and microfluidic cartridges.

Talentmark Stevenage, Hertfordshire, United Kingdom £60,000 – £80,000 pa