Latest regulatory affairs Jobs

Sr Director/Director and Team Lead, Global Regulatory Strategy - LCM

Leads the development and execution of global regulatory lifecycle strategies for assigned assets, aligning with integrated development plans and key market requirements. Works across GSK’s matrix structure to ensure regulatory compliance, supports commercial teams, and represents the company with health authorities. Provides strategic input into due diligence and crisis management while managing a team of regulatory professionals.

GSK Stevenage, United Kingdom

Sr Director/Director and Team Lead, Global Regulatory Strategy - LCM

Leads the development and execution of global regulatory lifecycle strategies for assigned assets, ensuring alignment with GSK's medicine development plans and regulatory requirements across key markets. Acts as the primary regulatory point of contact on cross-functional teams, drives innovation in regulatory approaches, and provides strategic input to business development and crisis management. Directly manages a team and collaborates with senior leaders and health authorities worldwide.

GSK United Kingdom

Hybrid Permanent

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

This role involves developing and maintaining global labelling strategies and core documentation for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will lead cross-functional discussions, ensure regulatory compliance, and translate clinical data into accurate, consistent labelling content for global markets. They will also support health authority interactions and contribute to risk assessment and audit readiness.

Novartis

Hybrid Permanent

Global Medical Affairs Director, Immunology

Lead the development and execution of global medical strategies for immunology products across their lifecycle, from development to market. Drive evidence generation through real-world studies, registries, and investigator-initiated trials while engaging key scientific experts and patient groups. Provide medical leadership at major congresses and advisory boards, ensuring compliance and strategic input into regulatory, access, and launch planning.

Novartis London, United Kingdom £93,870 – £174,330 pa

Manager, Global Regulatory Science CTA

Lead the end-to-end operational execution of Clinical Trial Applications (CTAs) outside the US, ensuring regulatory compliance and timely submissions across global markets. Serve as the subject matter expert on UK clinical trial regulations, including MHRA requirements and evolving legislation, while leveraging digital tools and AI-enabled technologies to enhance regulatory operations. Collaborate with cross-functional teams and CROs to maintain inspection-ready documentation and drive continuous improvement in regulatory processes.

Moderna Poland

On-site Permanent

Manager, Global Regulatory Science CTA

Lead the operational execution of Clinical Trial Applications (CTAs) globally outside the US, with a focus on compliance, submission excellence, and cross-functional coordination. Serve as the subject matter expert for the UK clinical trial regulatory landscape, including MHRA requirements and evolving legislation. Leverage digital platforms and AI-enabled tools to enhance regulatory operations and submission efficiency across international markets.

Moderna

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

Study Manager, Clinical Operations

Manages end-to-end clinical trial operations for 2–3 gene therapy studies, ensuring compliance with global regulatory standards and internal SOPs. Coordinates cross-functional teams, CROs, and vendors to deliver on timelines and budget, with responsibilities spanning protocol development, site selection, data integrity, and risk management. Focuses on patient safety, trial documentation, and operational planning within a rare disease gene therapy context.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

Scientist 2 - Analytical

Perform analytical testing on medical devices, skincare products, and raw materials using techniques like HPLC, FTIR, and ICP-MS. Support method development, validation, and compliance with ISO 13485 and GMP standards. Contribute to R&D projects, maintain laboratory equipment, and ensure accurate data reporting and documentation in a regulated environment.

Carbon 60 Deeside, Clwyd, United Kingdom £132 – £142 pd

On-site Contract

Associate Director, Facility & Validation Quality

Leads quality strategy and compliance for facility, equipment, utilities, and validation activities across the lifecycle from design to GMP operations. Ensures contamination control, sterility assurance, and regulatory alignment for a gene therapy manufacturing site. Works cross-functionally to support operational readiness, inspection preparedness, and compliant, risk-based decision-making in a regulated environment.

Orchard Therapeutics London, United Kingdom

Hybrid

Biomedical Field Service Engineer

This role involves performing preventative maintenance and repairs on medical equipment in UK hospitals, ensuring minimal disruption to hospital operations. You will work closely with the site manager, maintain service documentation, and interact with customers and OEM staff. The position requires strong communication skills and familiarity with regulatory standards.

Focus Resourcing United Kingdom

On-site Permanent

Study Director

Acts as a scientific lead overseeing regulated bioanalytical studies including pharmacokinetics (PK), anti-drug antibody (ADA), and biomarker analysis. Provides strategic direction and ensures compliance with GLP/GCP standards while serving as the primary point of contact for clients and internal teams. Focuses on high-quality scientific delivery within a collaborative, expanding biopharmaceutical lab environment.

VRS Recruitment Cambridge, United Kingdom £35,000 – £45,000 pa

Embedded Systems Engineer

Embedded Systems EngineerA long-established global manufacturer of high-voltage power solutions used in medical devices, semiconductor equipment, scientific instruments and industrial systems. The organisation operates design and manufacturing facilities across North America, Europe and Asia and partners with leading OEMs developing...

Terry Parris Associates Codmore Hill, West Sussex, RH20 1DQ, United Kingdom

Lab Manager

Manages laboratory operations and technical support teams in a regulated pharmaceutical environment, ensuring efficient operation of HPLC and GC systems, laboratory consumables, sampling, and waste management. Provides hands-on technical leadership, troubleshooting, maintenance coordination, and team development. Focuses on safety, compliance, and continuous improvement within a high-performance analytical lab setting.

VRS UK Irvine, Ayrshire And Arran, United Kingdom £40,000 – £42,000 pa