Latest regulatory affairs Jobs

ViiV Healthcare (GSK) Medical Director, ViiV R&D Physician Center of Excellence

The Medical Director role at ViiV Healthcare focuses on managing and overseeing Phase 1-4 clinical trials, ensuring the successful planning, execution, and reporting of protocols. Key responsibilities include providing medical governance, managing safety events, and collaborating with internal and external stakeholders to develop groundbreaking HIV treatments.

GSK

On-site Permanent

Medical Director, ViiV Healthcare

The Medical Director role at ViiV Healthcare involves managing and reporting data from Phase 1-4 clinical trials, contributing to protocol development, and providing medical oversight and support. You will work closely with internal and external stakeholders to ensure the successful execution and interpretation of clinical studies, with a focus on advancing HIV treatments and prevention.

GSK United Kingdom

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

Pfizer

On-site Permanent

Director, Search & Evaluation Early TA Lead

Two Directors of Search & Evaluation to lead strategic sourcing and evaluation of external innovation opportunities in Hematology, and Cardiovascular/Renal therapeutic areas. Embedded within each Therapeutic Area Leadership Team (TALT), these leaders will identify and advance high-potential assets from preclinical...

CSL

Director, Search & Evaluation Early TA Lead

Two Directors of Search & Evaluation to lead strategic sourcing and evaluation of external innovation opportunities in Hematology, and Cardiovascular/Renal therapeutic areas. Embedded within each Therapeutic Area Leadership Team (TALT), these leaders will identify and advance high-potential assets from preclinical...

CSL

Executive Director, Strategy, Oncology R&D

This role involves owning and driving the global Oncology R&D strategy, setting priorities for the senior executive team, and transforming the approach to deliver impact for patients. The Executive Director will lead the creation of comprehensive therapeutic area strategies, provide strategic recommendations to senior leadership, and collaborate across functions to drive innovation and impact.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Statistician (Scientist)

The role involves providing statistical support for manufacturing and analytical processes, using advanced data analytics and visualisation techniques. You will work across multiple teams to improve process understanding and drive data-driven decision-making, contributing to AstraZeneca's digital transformation.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

(Fixed-Term) Manufacturing Associate, Drug Substance - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology, with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization,...

Moderna Oxford, United Kingdom

(Fixed-Term) Manufacturing Associate II - Shift Position

The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...

Moderna Oxford, United Kingdom

Project Manager - Pharmaceutical

This role involves managing the installation, commissioning, and validation of a pharmaceutical facility expansion. You will lead cross-functional teams, ensure compliance with quality and safety standards, and contribute to continuous improvement. The projects are complex and require a structured approach in a regulated environment.

Smart4Sciences Surrey, United Kingdom £50 – £55 ph

On-site Contract

Business Analyst

The Business Analyst will support a key programme focused on the collection, tracking, and lifecycle management of human biological samples. Responsibilities include eliciting and documenting requirements, mapping end-to-end processes, and facilitating stakeholder workshops to enhance biobanking systems and data flows.

DCV Technologies Stevenage, Hertfordshire, United Kingdom £400 – £450 pd

Hybrid Contract

Complaints Investigator/ Quality Technician

This role involves hands-on device testing, deep-dive investigations into customer-returned medical devices, and using Excel to track quality trends. You will collaborate with global teams to improve product design and participate in continuous improvement projects, ensuring all findings meet strict regulatory standards.

Randstad Inhouse Services Witney, Oxfordshire, United Kingdom £16 ph

On-site Permanent Shift-work

Founding QMS Architect

This role involves architecting and implementing a lean, scalable Quality Management System (QMS) for a fast-paced, advanced manufacturing company. The QMS Architect will create compliance frameworks that accelerate delivery, coordinate with external regulatory specialists, and embed quality into the product lifecycle across multiple regulated industries.

KO2 Embedded Recruitment Solutions Reading, Berkshire, United Kingdom £80,000 – £100,000 pa

On-site Permanent

Production Scheduler

As a Production Scheduler, you will plan and coordinate production activities for multiple projects in a low-volume, R&D-focused medical device manufacturing environment. You will ensure efficient resource allocation, timely delivery, and compliance with ISO13485 standards, acting as a key liaison between manufacturing, supply chain, quality, and engineering teams.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £40,000 – £45,000 pa

On-site Permanent