Latest Pharmaceuticals Jobs

Quality Manager (on Shift)

The Quality Manager on Shift ensures compliance with GMP and regulatory requirements during manufacturing and non-manufacturing activities. Key responsibilities include monitoring quality systems, investigating deviations, and supporting product release. The role involves working in a 24/5 shift pattern, including weekends, and promoting team collaboration and continuous improvement.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

Specialist - Extractables and Leachable - MSAT EM

This role involves leading Extractables and Leachables (E&L) assessments for biopharmaceutical manufacturing processes, container closure systems, and dosing devices. The Specialist will work with internal and external labs to ensure E&L testing is completed scientifically, compliantly, and cost-effectively, while also managing risk identification and escalation.

GSK East Hertfordshire, United Kingdom £70,650 – £117,750 pa

On-site Permanent

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and AI/ML infrastructure, focusing on reliability, scalability, and security. Key responsibilities include architecting and operating scalable cloud platforms using AWS services, defining reusable infrastructure patterns, and mentoring engineers to improve deployment reliability and operational maturity.

Pfizer

On-site Permanent

Staff Platform Engineer, AI/ML Infrastructure

The Staff Platform Engineer, AI/ML Infrastructure will lead the technical strategy for cloud platforms and deployment systems that power enterprise-scale generative AI applications. Responsibilities include defining infrastructure architecture, building scalable cloud platforms using AWS services, and improving CI/CD, observability, and security practices.

Pfizer

On-site Permanent

SERM Medical Director

The SERM Medical Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. Key responsibilities include interpreting safety data, managing safety signals, and providing expert medical input to support benefit-risk decisions. This role involves leading cross-functional teams, collaborating with regulatory authorities, and shaping the safety strategy for innovative oncology medicines.

GSK

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, mentoring staff, and engaging with external agencies to ensure compliance and expedite submissions.

GSK Canterbury, United Kingdom

On-site Permanent

Senior Manager - CMC Regulatory Affairs Biopharm Development Projects

This role involves leading CMC regulatory activities for GSK's investigational, late development, and early commercial products. Responsibilities include driving CMC strategy, preparing regulatory documents, managing project activities, and mentoring staff. The position requires a strong understanding of regulatory requirements and the ability to communicate complex issues across departments and with external agencies.

GSK

On-site Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.

GSK Stevenage, United Kingdom

Hybrid Permanent

SERM Scientific Director

This role involves leading pharmacovigilance and risk management for GSK's global assets, ensuring scientifically sound review and interpretation of safety data. The director will develop and execute safety strategies, manage safety governance, and lead cross-functional teams to address product safety issues and ensure patient safety globally.

GSK

On-site Permanent

SERM Scientific Director

The SERM Scientific Director role involves leading pharmacovigilance and risk management planning, developing safety strategies, and ensuring the scientific soundness of data reviews. The position requires expertise in evaluating safety risks, managing cross-functional teams, and communicating safety issues to senior management.

GSK

On-site Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities, develop and execute oncology clinical trials, and engage with key external experts. Responsibilities include protocol development, medical monitoring, safety data review, and collaborating with various stakeholders to advance GSK’s clinical portfolio.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.

GSK United States

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research activities for GSK’s oncology portfolio, including developing and executing phase 1-3 clinical trials. They will collaborate with various stakeholders to ensure high-quality protocol development, medical monitoring, and data interpretation, while also engaging with key external experts and thought leaders.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research and development of GSK’s oncology portfolio, collaborating with various stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include medical oversight, protocol development, data interpretation, and engagement with key external experts to ensure the successful regulatory filing and market launch of innovative oncology treatments.

GSK

Hybrid Permanent