Latest Pharmaceuticals Jobs

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Head of DMPK

The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.

Recursion United Kingdom

Hybrid Permanent

Audit Senior Lead (EMEA GMP Audit)

The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.

GSK

On-site Permanent

Audit Senior Lead (EMEA GMP Audit)

This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.

GSK

Hybrid Permanent

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

VP & Global Head, Discovery Chemistry and DMPK, Oncology Targeted Delivery

This role involves leading the global Discovery Chemistry and DMPK function within AstraZeneca's Oncology Targeted Delivery (OTD) organization. Responsibilities include setting strategic direction, driving innovation in small molecules, ADCs, and RCs, and fostering a high-performing, collaborative culture across R&D sites in Cambridge (UK), Cambridge (MA), and Gaithersburg (US).

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Scientist – Peptide Chemistry

This role involves conducting laboratory-based experimental work in peptide chemistry, designing and synthesizing peptides using solid-phase techniques, and contributing to the development of new peptide medicines. The position offers opportunities for personal and professional growth within a dynamic and collaborative team.

AstraZeneca Cambridge, United Kingdom

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

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 activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

This role involves leading the development and submission of regulatory documents, providing strategic direction, and negotiating with health authorities to expedite approvals. The position also focuses on ensuring compliance and timely approval of new and marketed products, serving as a regulatory liaison throughout the product lifecycle.

Novartis London, United Kingdom

Hybrid Permanent

Global Labelling Manager, Content

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels and regulatory guidance, and ensuring compliance with global standards across the product lifecycle.

Novartis London, United Kingdom

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