Latest Medical Devices Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.

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 shaping regulatory approaches and mentoring teams in a complex, science-driven environment.

GSK €90,000 – €150,000 pa

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing strategies to enhance Pfizer's medical insights capabilities. Key responsibilities include developing insights frameworks, driving alignment across medical affairs, and leveraging advanced analytics and AI to translate complex data into actionable insights that inform strategic decisions.

Pfizer

On-site 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 advanced analytics, AI, and emerging technologies to inform Pfizer's medical strategies and improve the value of medical insights.

Pfizer

On-site Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

This role involves leading strategic sourcing and evaluation of external innovation opportunities in Hematology and Cardiovascular/Renal therapeutic areas. Responsibilities include identifying high-potential assets, shaping early partnering strategies, and driving transactions in collaboration with Business Development. The role requires deep scientific expertise and a strong network within biotech, academia, and pharma BD organizations.

CSL

On-site Permanent

Director Biostatistics - Hematology

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...

CSL

Senior Principal Biostatistician

This role involves leading the implementation of innovative trial designs and statistical models, collaborating with clinical and regulatory teams, and contributing to exploratory analyses and statistical consultations. The position requires a strong background in biostatistics and the ability to drive quantitative decision-making in clinical trials.

Novartis London, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Engineering Technician

The Engineering Technician role involves providing comprehensive engineering support for the Steriles Business Unit, focusing on equipment maintenance, GMP compliance, and continuous improvement initiatives. Responsibilities include breakdown repairs, calibration, quality documentation, and project support, all while maintaining high safety and regulatory standards.

GSK Barnard Castle, United Kingdom

On-site Permanent Shift-work

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Process Engineer

The Process Engineer role involves providing technical expertise to support safe and efficient manufacturing at GSK's Montrose site. Responsibilities include resolving technical issues, contributing to capital projects, improving process plant software, and collaborating with cross-functional teams to ensure compliance and process improvements.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

On-site Contract

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for regulatory and research purposes. Working closely with statisticians and data scientists, the role involves developing validated datasets, tables, listings, and figures using CDISC standards such as SDTM and ADaM, while ensuring compliance with GxP and ICH guidelines. The position supports agile delivery within a hybrid work environment and emphasizes technical excellence, collaboration, and innovation in clinical data programming.

GSK Stevenage, United Kingdom

Hybrid Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent