Latest regulatory affairs Jobs

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, leading resource planning, and representing the function in senior interactions and health authority meetings.

AstraZeneca United States

On-site Permanent

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Regulatory Conformance Specialist

This role involves ensuring regulatory compliance for pharmaceutical manufacturing by interpreting cGMP, QMS, and pharmacopoeial standards. The specialist supports product lifecycle changes, leads NPI submissions, maintains quality specifications, and acts as the site's regulatory liaison, handling audits and compliance deviations across a high-volume production environment.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

Global Program Regulatory Manager - Neuroscience

This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing and submitting clinical trial applications, managing health authority interactions, and ensuring compliance throughout the product lifecycle. The manager will work cross-functionally to translate scientific data into regulatory submissions and support timely approvals. It is a hybrid role based in London, requiring strong expertise in pharmaceutical regulatory affairs.

Novartis

Hybrid Permanent

Regulatory Intelligence Lead - Biologics/Vaccines

Leads global regulatory intelligence strategy for biologics and vaccines, interpreting evolving cGMP regulations and shaping policy to support Pfizer’s quality and compliance standards. Represents the company in international forums, influences regulatory guidelines, and drives digital transformation of intelligence capabilities. Works across global teams to ensure alignment on compliance and quality initiatives for innovative therapies.

Pfizer Belgium

On-site Permanent

Regulatory Intelligence Lead - Biologics/Vaccines

Leads global regulatory intelligence strategy for biologics and vaccines, interpreting evolving cGMP regulations and shaping policy to support Pfizer's compliance and innovation goals. Represents the company in international forums, influences regulatory standards, and drives digital transformation of intelligence capabilities. Works across quality, regulatory, and technical teams to ensure global alignment and inspection readiness.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Quality and Regulatory Labelling Program Manager

This role involves leading global labelling initiatives to ensure compliance with regulatory standards across multiple markets. The Program Manager will work closely with cross-functional teams to manage change controls, mitigate risks, and drive continuous improvement in labelling processes.

Randstad Engineering Popley, Hampshire, RG24 9TW, United Kingdom £27 ph

Hybrid Contract

Associate Director, Regulatory Diagnostics

Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Vice President, Medical Affairs

As Vice President, Medical Affairs, you will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare diseases, and immunology. You will collaborate with cross-functional teams to build evidence, engage key stakeholders, and ensure the translation of scientific insights into meaningful patient impact.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

PV Systems and Processes Lead x2

This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.

CSL United Kingdom

On-site Permanent

Technical Writer

The Technical Writer will create and maintain technical and customer-facing documents, working closely with teams in Regulatory Affairs, Marketing, and Technical Services. The role involves ensuring accuracy and up-to-date information, supporting continuous improvement, and maintaining customer and product data in company systems.

Talentmark Burgess Hill, West Sussex, United Kingdom £264 – £331 pd

Hybrid Contract Clearance Required

Plant Quality Manager

Lead quality assurance and control operations at a regulated manufacturing site producing both cosmetic and medical device products. Oversee compliance with GMP, ISO 13485, and ISO 22716 standards, support audits, and drive continuous improvement initiatives. Collaborate with cross-functional teams including operations, engineering, regulatory affairs, and R&D to ensure product quality and regulatory alignment.

New Appointments Group Folkestone, Kent, United Kingdom

On-site Permanent

Director, Clinical Pharmacology

This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs. Responsibilities include designing clinical studies, authoring regulatory documents, and collaborating with cross-functional teams to expedite drug development.

Recursion North Tyneside, NE29 8EP, United Kingdom US$212,900 – US$297,000 pa

Hybrid Permanent

QA/RA Manager

This role involves leading the design and implementation of regulatory and quality management systems for a portfolio of Class I medical devices, ensuring compliance with ISO 13485 and 21 CFR 820. The candidate will oversee digital EQMS deployment, lead audits, manage post-market surveillance, and build a distributed team while embedding a proactive compliance culture across R&D, supply chain, and commercial functions.

SRG London, United Kingdom

Hybrid Permanent