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A leading organisation in the biopharmaceutical sector is seeking a Project Manager Quality to oversee quality-related projects and drive continuous improvements within a dynamic and regulated environment. This role offers an exciting opportunity to contribute to the enhancement of quality systems, compliance processes, and operational efficiencies while collaborating with cross-functional teams.

A leading organisation in the pharmaceutical sector is seeking an Analytical Sciences & Technology (AST) Analyst to support key analytical projects and ensure compliance with Good Laboratory Practices (cGLP). This role presents an exciting opportunity to contribute to method development, qualification, and troubleshooting within a dynamic and collaborative environment. As a vital member of the AS...

A leading global organisation is seeking a Head of Alliance Quality, an experienced quality professional with a strong background in manufacturing, compliance, and contract management. This role offers an exciting opportunity to oversee and enhance external supply operations, ensuring alignment with global Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) standards. As a key ...

A leading organization is seeking an experienced Head of Medical Clinical Science to drive clinical research and medical strategy within a transformative and innovative environment. This senior role offers an exciting opportunity for a medical professional to lead impactful clinical studies, ensuring scientific excellence and regulatory compliance. As a key member of the Clinical Research and Dev...

GxPeople Global is partnering with a leading global consumer goods company to identify their next Medical Safety Officer—a highly skilled professional with a strong background in clinical trial safety and pharmacovigilance. This role presents an exciting opportunity for an experienced medical professional to take on a key position ensuring patient safety across pre-market and post-market activitie...

GxPeople Global is partnering with a leading global consumer goods company to find their next Senior Clinical Scientist. This role offers an exciting opportunity for an experienced professional to contribute to early-phase clinical research, with a strong focus on Phase 1 trials and PK/PD studies. You will work in a collaborative, high-impact environment, supporting clinical trial design, executio...

GxPeople Global is partnering with a well-established Medical Device Manufacturer & Supplier to find their next senior leader—a Head of Regulatory Affairs. This is a pivotal moment for the business as they transition from the Medical Device Directive (MDD) to the Medical Device Regulation (MDR), making this role a key strategic appointment.

GxPeople Global are looking for a QMS Engineer to join a well-established Medical Device manufacturer based in Oxford to join their Quality team.

GxPeople is partnering with a highly reputable Quality Consultancy to find their next team member—a Qualified Person (QP) who thrives in a dynamic environment and enjoys working on diverse projects. This role offers an excellent opportunity for an experienced QP to leverage their expertise across multiple clients, gaining exposure to a wide range of products and regulatory frameworks. As a senior...

GxPeople Global is seeking a QARA Associate to join a leading Medical Device company in Surrey. Our client is an Employee-Owned organisation, where every team member has a voice in shaping the company’s future. This is a full-time hybrid position, offering a balance of on-site collaboration and remote flexibility.

The Head of Corporate QMS will lead the development, implementation, and oversight of the Global Quality Management System (QMS), ensuring compliance with international standards and promoting a culture of continuous improvement. Reporting to the Chief Quality Officer.

The Head of Corporate Quality will oversee Quality Assurance (QA) across Product Development, Pharmacovigilance, and Regulatory Affairs, ensuring compliance with international standards. The role will drive quality improvements, manage regulatory requirements, and promote a strong culture of quality throughout the organization.