Latest Pharmaceutical Scientist Jobs

SERM Scientific Director, Oncology

The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.

GSK United Kingdom

Hybrid Permanent

SERM Scientific Director

The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.

GSK

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This role involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

On-site Permanent

Senior Director of Operational Technology (Operations)

This role involves leading the execution of OT strategy across AstraZeneca's global manufacturing network, ensuring alignment with business priorities and improving reliability, safety, and compliance. Key responsibilities include lifecycle management, risk mitigation, capability building, and regulatory readiness.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Director, Alliance Management

This role involves leading strategic partnerships with CROs, ensuring governance, performance, and relationship management. The Director will collaborate globally, drive continuous improvement, and support cross-functional teams at AstraZeneca's Cambridge Biomedical Campus.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Deviation Owner

This role involves leading the investigation and resolution of manufacturing deviations in a GMP-regulated environment, ensuring compliance and product quality. The Deviation Owner will coordinate root cause analyses, drive corrective actions, and work across quality, production, and engineering teams to prevent recurrence. Emphasis is placed on data-driven problem solving, governance of deviation processes, and continuous improvement through structured methodologies like DMA/IC.

GSK Barnard Castle, United Kingdom

On-site Permanent

Operations NPI Technologist

This role involves leading the integration of new equipment, processes, and technologies into sterile manufacturing operations, ensuring compliance, safety, and minimal disruption to supply. The technologist will work across project lifecycles—from design and validation to handover—providing technical leadership and operational readiness support. Collaboration with engineering, quality, and digital manufacturing teams is key to deploying capital projects and new product introductions in a GMP-regulated environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Technical Operations Manager

Lead technical operations at a UK pharmaceutical manufacturing site, ensuring safe, compliant, and efficient production of medicines. Provide technical leadership, resolve process and equipment issues, and drive continuous improvement in a GMP-regulated environment. Collaborate with engineering, quality, and supply chain teams to maintain operational excellence and support audit readiness.

GSK Barnard Castle, United Kingdom

On-site Permanent

Projects Operations Manager

Leads project operations at a UK pharmaceutical manufacturing site, ensuring safe, compliant, and efficient delivery of capital projects, new product introductions, and process changes. Works cross-functionally with engineering, quality, and operations teams to manage resources, resolve constraints, and maintain GMP and safety standards throughout project lifecycles.

GSK Barnard Castle, United Kingdom

On-site Permanent

Process Safety Engineer

This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Device Technologist - 12 Month Secondment

The Device and Packaging Technologist provides technical support for device assembly and packaging activities, including new product introduction, change control, and continuous improvement. The role involves collaborating with site teams, central technology functions, and external suppliers to ensure compliant and efficient solutions throughout the product lifecycle.

GSK Barnard Castle, United Kingdom

On-site Contract

Inspection Assembly & Packaging Operations Manager

You will lead inspection, assembly, and packaging operations at a GSK site in the UK, managing day-to-day production, quality, and safety while coaching your team to improve. You will work closely with quality, engineering, and supply chain colleagues to deliver on-time, compliant output and drive continuous improvement projects.

GSK Barnard Castle, United Kingdom

On-site Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents, leading cross-functional teams, and managing complex writing projects. The Principal Medical Writer will interpret clinical and statistical data, ensure compliance with regulatory requirements, and contribute to global regulatory submissions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK United Kingdom

Hybrid Permanent