Latest regulatory affairs Jobs

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for drug development and approval, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation within the regulatory framework.

GSK United Kingdom

Hybrid Permanent

Manager, Global Regulatory Strategy, Oncology

This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.

GSK

Hybrid Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, ensuring patient-centered, evidence-driven decisions, and leading interactions with clinical and research experts. The role requires deep oncology expertise and strong leadership to drive medical impact globally.

Pfizer

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer Sandwich, United Kingdom

On-site Permanent

Global Regulatory Associate Director, Life Cycle Management

Manages regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. Develops strategic input on safety reports, variations, and renewals, while leading responses to regulatory queries and supporting cross-functional initiatives. Plays a key role in lifecycle management of innovative medicines, requiring strong scientific interpretation and stakeholder collaboration.

Novartis £67,900 – £126,100 pa

Hybrid Permanent

Associate Director, Biostatistics

This role leads the statistical strategy and execution for clinical development programs within a therapeutic area, ensuring robust study design, data analysis, and regulatory compliance. The Associate Director collaborates with cross-functional teams, represents biostatistics in regulatory interactions, and oversees internal or outsourced programming efforts. They also drive innovation in statistical methodologies and contribute to clinical trial interpretation and reporting.

CSL

Hybrid Permanent

(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

(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

Translational Medicine Expert – Dermatology, Associate Director

This role involves leading translational medicine strategies in dermatology, spanning early to late-stage drug development. The expert will drive clinical pharmacology, biomarker development, and regulatory strategies while collaborating across research, development, and external stakeholders. Key responsibilities include study design, safety oversight, and scientific leadership in global project teams.

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

Hybrid Permanent

Quality Lead

This role involves leading quality and regulatory compliance for a multinational manufacturer across Europe and Africa, with a focus on medical devices and consumer products. The candidate will oversee the Quality Management System, drive product launches, conduct audits, and ensure adherence to standards like MDD/MDR, ISO 13485, and MHRA. It requires a technically strong quality professional who can lead cross-functionally and balance strategic oversight with hands-on problem-solving.

New Appointments Group Folkestone, Kent, United Kingdom

On-site Permanent

QC Analyst

This role involves hands-on analytical testing and data reporting for raw materials, intermediates, and finished products within a GMP-regulated laboratory. The analyst ensures compliance with ALCOA+ data integrity standards, investigates deviations and out-of-specification results, and supports continuous improvement in quality control processes. It is a detail-oriented position focused on maintaining regulatory compliance and laboratory accuracy.

Smart4Sciences Almere Stad, Netherlands

On-site Permanent

Clinical & Validation Principal

Lead bioanalytical method development and validation activities within a GxP-regulated laboratory, overseeing HPLC, UPLC, and LC-MS/MS platforms. Manage a technical team, ensure regulatory compliance, and support audits and submissions. Focus on method optimisation, troubleshooting, and continuous improvement in a highly controlled environment.

Next Phase Recruitment Armagh, County Armagh, United Kingdom

On-site Permanent

Senior Scientist or Associate Principal Scientist Metabolist Team

This role involves conducting advanced in vitro and ex vivo research to identify and validate therapeutic targets for obesity. The successful candidate will work in a dynamic, collaborative environment, designing and implementing experiments, analyzing data, and contributing to drug discovery projects across multiple sites.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development of a medicine for cardiovascular and renal conditions, managing a cross-functional team, and ensuring compliance with regulatory standards. Responsibilities include strategic planning, clinical oversight, and authoring key documents for regulatory submissions and publications.

CSL Switzerland

On-site Permanent

Associate Director Integrated Bioanalysis – Biopharma Bioanalytical Program Lead

This role involves leading the bioanalytical strategy for diverse therapeutic modalities, collaborating with global project teams to develop robust assays, and translating complex data into clear program decisions. The position is highly visible, requiring cross-functional influence and external representation of scientific findings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent