Latest Medical Devices 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 across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.

GSK £144,375 – £240,625 pa

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring consistency and value across Pfizer’s medical portfolio.

Pfizer

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role at Pfizer involves shaping and implementing Medical Insights processes, collaborating with various stakeholders, and leveraging advanced analytics and AI to translate complex medical data into actionable insights. The role focuses on embedding these insights into medical decision-making and strategic discussions, ensuring they are relevant and impactful across Pfizer’s portfolio of medicines.

Pfizer

Remote 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

Global Labelling Director, Content (Immunology)

The Global Labelling Director, Content (Immunology) will lead the development and delivery of high-quality global labelling strategies for innovative medicines. Key responsibilities include developing core labelling documents, collaborating with cross-functional teams, and ensuring compliance with regulatory requirements. The role involves representing global labelling in governance forums and contributing to decision-making discussions.

Novartis

Hybrid Permanent

Clinical Development Director - Renal

The Clinical Development Director is responsible for leading and supporting the delivery of clinical deliverables for a section of a global clinical program or a large, complex trial. This role involves collaborating with various teams to ensure data quality, regulatory compliance, and scientific accuracy in clinical trials and publications.

Novartis London, United Kingdom

Hybrid Permanent

Director, CMC Regulatory Affairs

Leads global CMC regulatory strategy for small molecule medicines, shaping development and approval pathways across international markets. Works at the intersection of R&D, supply, quality, and commercial functions to ensure regulatory compliance and uninterrupted patient access. Focuses on solving complex regulatory challenges, mentoring talent, and improving processes to support long-term product success.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Process Technologist

As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.

GSK Barnard Castle, United Kingdom

On-site Permanent

Research Pipeline Project Manager

The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in team efficiency and transparency.

GSK Stevenage, United Kingdom

Hybrid Permanent

Principal Programmer / Analyst

The Principal Programmer / Analyst role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering innovation and quality assurance in a global, agile environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

This role involves managing and improving stability data for small molecule studies, creating and maintaining study protocols, and producing clear data visualizations for regulatory submissions. You will work closely with cross-functional teams and external partners to drive process improvements and ensure data integrity.

GSK Stevenage, United Kingdom

Hybrid Permanent

Scientist, Analytical Operations - Small Molecule Stability Data Management

In this role, you will manage and improve stability data for small molecule studies, create and maintain study protocols, collect and analyse datasets, and produce clear summaries and visualisations for regulatory submissions. You will also support audits, collaborate with cross-functional teams, and drive process improvements through digital tool adoption.

GSK East Hertfordshire, United Kingdom

Hybrid Permanent