Latest Pharmaceuticals Jobs

Staff Engineer, AI Security and Product Security

This role involves leading product and AI security strategy across web, mobile, API, cloud, and container environments with a strong shift-left approach. The engineer will secure AI/ML systems, including LLM integrations, agentic pipelines, and MLOps infrastructure, while defending against AI-specific threats like prompt injection and model extraction. They will also drive secure development practices, conduct threat modeling, and lead incident response in collaboration with cross-functional teams.

Recursion United Kingdom US$186,900 – US$220,400 pa

Hybrid Permanent

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharm, vaccines, and pharmaceutical facilities. Responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports. The role requires strong communication skills and subject matter expertise in sterile manufacturing.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across EMEA and other highly regulated markets. Responsibilities include evaluating compliance, conducting various types of audits, and producing clear audit reports to inform senior management of identified risks and corrective actions.

GSK

Hybrid 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

Medical Director, Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, evaluating safety data, and managing risk to patients. You will work closely with regulatory agencies, contribute to global submissions, and ensure the safety and efficacy of AstraZeneca's products throughout their lifecycle.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Medical Director, Senior Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent Flexible

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site 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

Global Program Safety Team Lead - Neuroscience

This role involves leading medical safety strategy for neuroscience drug development programs at Novartis, managing global cross-functional teams, and ensuring robust benefit-risk evaluation throughout the product lifecycle. The position requires deep expertise in safety signal detection, regulatory submissions, and mentoring safety professionals, with a strong focus on clinical development and lifecycle management. Based in London or remotely, the role plays a key part in shaping global safety standards and driving patient-centric innovation.

Novartis London, United Kingdom £104,790 – £194,610 pa

Hybrid Permanent

Cluster HTA Hub Senior Manager

In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans to enhance the value of Pfizer's medicines. You will collaborate with sales teams and utilize health economic models to maximize sales and improve customer interactions.

Pfizer Poland

On-site Permanent

Cluster HTA Hub Senior Manager

In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans. You will also collaborate with sales teams to maximize sales and enhance customer interactions using health economic models.

Pfizer London, N1 5EA, United Kingdom

Hybrid Permanent

Senior Production Operator

This role involves producing medical devices in a Grade C cleanroom, following strict SOPs and quality standards. Responsibilities include in-process inspections, maintaining production records, and contributing to process improvements.

THOMAS Professional Mitton, Gloucestershire, GL20 8AW, United Kingdom £32,000 – £38,000 pa

On-site Permanent