Latest regulatory affairs Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex international environments.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven decisions. The position requires deep oncology expertise and leadership to drive medical impact across international markets.

Pfizer

On-site 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 high-quality medical execution across regions. The role requires deep oncology expertise, strategic thinking, and collaboration with global and regional stakeholders to drive the oncology scientific narrative and data interpretation.

Pfizer

On-site Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. The candidate will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous improvement initiatives. It's a key position influencing patient access to medicines through robust lifecycle management.

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

Hybrid Permanent

Director, Medical Evaluation & Case Processing Oversight

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an...

CSL

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent

Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays

This role involves hands-on development, qualification, and validation of functional immunoassays to support mRNA-based clinical trials. The scientist will generate and analyze high-quality data in a GCP-compliant lab environment, contribute to assay innovation, and ensure regulatory compliance. Collaboration with cross-functional teams and use of digital tools, including AI-enabled platforms, are integral to supporting clinical development objectives.

Moderna

On-site Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data from clinical samples in compliance with GcLP standards, using platforms like Watson LIMS and electronic lab notebooks. The position emphasizes regulatory compliance, critical reagent management, and collaboration with cross-functional teams to deliver high-quality bioanalytical data for clinical programs.

Moderna

Hybrid Permanent

Laboratory Scientist - In-Vitro – Preclinical

This role involves supporting in-vitro and pre-clinical studies to generate scientific data for product safety assessment and regulatory submissions. The scientist will conduct biological assays, maintain lab operations, and contribute to data analysis within a multidisciplinary research environment. Work focuses on cell biology, toxicology, and pharmacology using cutting-edge methodologies.

Hudson Shribman United Kingdom £40,000 pa

On-site Contract

Quality Engineer

As a Q&RA Engineer, you will support quality and regulatory compliance in a highly regulated life sciences environment. You will lead deviation investigations, manage change control, and collaborate with cross-functional teams to maintain and improve quality systems, ensuring products meet stringent standards.

Hays Life Sciences Cheap, City And County Of the City Of London, United Kingdom

Hybrid Contract Flexible

Quality Engineer, Medical Devices

This role involves managing quality assurance processes within the medical devices sector, including developing documentation, conducting internal audits, and resolving customer complaints. The engineer will ensure compliance with ISO standards and support regulatory requirements in a company focused on innovative diagnostic systems. The position plays a key part in maintaining quality across a product range used in healthcare laboratories.

TRS Consulting Bolton, Manchester, M26 1HG, United Kingdom £40,000 – £50,000 pa

On-site Permanent

Quality Engineer, Medical Devices

This role involves managing quality systems for medical devices, including creating documentation, conducting internal audits, and handling customer complaints. The engineer will ensure compliance with regulatory standards such as ISO 13485 and ISO 9001 within a leading healthcare diagnostics company. The position supports product innovation and quality assurance in a highly regulated environment.

TRS Consulting Preston, East Riding Of Yorkshire, East Riding Of Yorkshire, HU12 8SB, United Kingdom £40,000 – £50,000 pa

On-site Permanent

QC Analyst – Pharmaceuticals

This role involves performing routine and non-routine analysis of raw materials and finished pharmaceutical products using techniques such as HPLC, GC, UV, and FTIR. The analyst will lead Out of Specification investigations, ensure compliance with GMP standards, and contribute to method development and validation. It is a site-based laboratory position requiring strong documentation, troubleshooting, and analytical skills in a regulated environment.

RBW Consulting New Malden, London, KT3 3JQ, United Kingdom

On-site Permanent