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

Team Lead, Therapeutic Area Quality

The Team Lead, Therapeutic Area Quality, leads a team of Quality Business Partners, ensuring quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the global audit plan. The role also involves talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include evaluating quality strategies, driving continuous improvements, and supporting health authority inspections. The role also focuses on talent development and maintaining expertise in international regulations.

GSK

On-site Permanent

Team Lead, Therapeutic Area Quality

This role involves leading a team of Quality Business Partners to ensure quality is integrated into R&D programs and projects. Responsibilities include driving quality improvements, supporting health authority inspections, and contributing to the quality strategy and risk management. The role requires a deep understanding of regulatory requirements and the ability to lead a global quality team.

GSK

On-site 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

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory submissions. The position requires strong technical expertise, collaboration across functions, and a focus on quality and compliance.

GSK East Hertfordshire, United Kingdom

On-site Permanent

MSAT Drug Product Lead (Parenteral Products)

This role involves managing the technical delivery of drug product manufacturing, primarily for GSK's sterile injectable products. Responsibilities include leading New Product Introduction (NPI), technology transfers, process verification, and regulatory compliance. The position requires strong technical expertise, collaboration across functions, and a focus on quality and patient safety.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Director, Translational Science Lead

This role leads translational science strategy across renal, inflammation, fibrosis, and neurodegeneration disease areas, driving biomarker development and validation to support clinical decision-making from preclinical through to launch. The position integrates cutting-edge technologies like spatial transcriptomics and human multi-omics data, working across discovery and development to de-risk clinical transitions and identify responder populations.

GSK Stevenage, United Kingdom US$178,200 – US$297,000 pa

Hybrid Permanent

Director, Translational Science Lead

Leads translational science strategy for renal, inflammation, fibrosis, and neurodegeneration programs, driving biomarker development and validation from preclinical to clinical stages. Focuses on integrating multi-omics data, human assays, and novel technologies to inform clinical decision-making and patient stratification. Works across discovery and development to advance differentiated therapeutics through cross-functional collaboration and external partnerships.

GSK Canterbury, United Kingdom £178,200 – £297,000 pa

Hybrid Permanent

Programming Leader

The Programming Leader role involves overseeing project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion the adoption of agile principles and new technologies to improve efficiency and data analysis.

GSK Stevenage, United Kingdom

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating submissions and ensuring compliance with global regulations. Works across cross-functional teams to address complex regulatory challenges and support continuous supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a matrix environment.

GSK Stevenage, United Kingdom €90,000 – €150,000 pa

Hybrid Permanent

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for pharmaceutical 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 risk mitigation, process improvement, and influencing regulatory decisions across complex projects.

GSK London, United Kingdom £90,000 – £150,000 pa

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent