Latest Professional Services Jobs

Associate Director, Global Regulatory Science, CMC

Lead global regulatory CMC strategy and submissions for mRNA-based medicines, ensuring compliance with international regulations. Guide cross-functional teams on regulatory requirements and oversee documentation for biologics across vaccine, oncology, and rare disease programs. Drive process improvements and interact directly with health authorities to support product development.

Moderna London, United Kingdom

Hybrid Permanent

Associate Director, Global Regulatory Science, CMC

Lead global CMC regulatory strategy for mRNA medicines, guiding international submissions and ensuring compliance with health authority requirements. Collaborate with manufacturing and quality teams to support product development across vaccines, oncology, and rare diseases. Develop and maintain regulatory documentation in CTD format, while driving process improvements and change control assessments.

Moderna

Hybrid Permanent

Associate Director, Global Publications & Foundational Content

Salary Range:£67,900.00 - £126,100.00Job Description SummaryAre you passionate about transforming complex scientific data into publications that shape healthcare and improve patient outcomes worldwide? As an Associate Director, Global Publications & Foundational Content, you will lead the development of high-impact scientific...

Novartis London, United Kingdom

NPI Quality Engineer

This role involves leading quality assurance throughout the new product introduction (NPI) process in a high-tech manufacturing environment. The engineer will ensure compliance with quality standards across design, development, and production, working closely with engineering, R&D, and supply chain teams. Key responsibilities include managing APQP/PPAP deliverables, leading root cause investigations, and driving continuous improvement in quality processes.

Yolk Recruitment Briton Ferry, West Glamorgan, SA11 2NH, United Kingdom £45,000 pa

On-site Permanent

Biologics Account Manager

This role involves driving adoption of respiratory biologics within secondary care settings by building strategic relationships with multi-disciplinary teams and key healthcare stakeholders. The Account Manager will lead formulary access, support homecare utilization, and execute account plans in a complex clinical environment. It requires strong commercial acumen, deep understanding of the NHS ecosystem, and the ability to navigate multi-stakeholder decision-making units.

AstraZeneca Sheffield, 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, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, 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 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

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Senior Scientist New Modalities, Analytical

This role involves defining and delivering analytical strategies for new modality medicines, such as peptides and oligonucleotides, from early development to commercial launch. You will work closely with cross-functional teams to ensure robust quality control, regulatory compliance, and efficient commercial supply, while leveraging digital tools and AI to enhance decision-making and process robustness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of CMC regulatory strategy for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and regulatory best practices. Support clinical trial materials and GMP inspections, ensuring alignment with evolving global regulations.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of global CMC regulatory strategies for small molecule drugs in clinical trials and marketing applications. Author and manage high-quality regulatory submissions across the US, EU, and rest of world, while advising cross-functional teams on compliance, risk mitigation, and evolving GMP standards. Collaborate closely with internal and external stakeholders to ensure timely delivery of regulatory deliverables and support clinical development programs.

Recursion London, W1C 2QP, United Kingdom

Remote 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 regional and global regulatory leads, partnering with directors on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca

On-site Permanent