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Looking for a diligent PowerBI Report Writer to join our Analytics department in the Life Science industry. The role involves developing, maintaining and improving reporting solutions for our Milton Keynes based team.
This Senior Quality Analyst role is a fantastic opportunity for a dedicated professional to ensure the highest quality standard in the Life Sciences industry. The position requires the application of exceptional analytical skills within the QC department.
This role as a Senior Clinical Quality Assurance Associate is crucial in maintaining and enhancing the quality standards of successful clinical trial delivery. You will be responsible for ensuring active participation in continuous quality improvement activities, working closely with Clinical Operations and other supporting areas.
This role will involve leadership of the Quality function, and its associated teams. The main areas of focus will be in driving compliance to GMP, as well as improving current processes and practices.
A fantastic opportunity utilisng scientific expertise to enhance robustness and accuracy of scientific operations and lab activities. You will be a Principal / Technical Lead responsible for ensuring client needs are met and projects delivered across clinical research, in line with regulated standards.
We are looking to speak to Quality Managers with Laboratory experience, who may be interested in joining a leading food testing laboratory based in High Wycombe.
We are seeking a detail-oriented Project Coordinator to assist with all aspects of labelling coordination within the labelling department. The ideal candidate will have a passion for detail, a high level of organisational skills, and high levels of administration experience.
This role offers an exciting opportunity for a Regulatory Affairs Manager to oversee and deliver regulatory strategies within the Pharmaceutical industry. The successful candidate will be responsible for managing regulatory activities and ensuring compliance with regulatory requirements.
We are seeking a full time permanent QP to join our client based in Newcastle. This is a great opportunity for anyone seeking a fresh challenge, with an innovative and fast growth business.
In this role, the Senior RAQA Consultant will work closely with Clients, implementing Quality Management Systems, Clinical Design Controls, and full software lifecycle process.
This Senior Quality Assurance Associate position demands a candidate with a good understanding of the GDP and GMP, who is capable of working as part of a team to ensure the highest standards of quality and safety are maintained.
An ideal role for someone experienced within QA/QC roles working to ISO17025
We are currently seeking a committed and experienced Senior Manager RAQA for a global leader within medical devices. The ideal candidate should possess a keen interest in quality assurance and regulatory affairs, with the ability to manage and lead the team effectively.
We are seeking a meticulous and dedicated Senior Regulatory Affairs Associate with a strong background in Regulatory Affairs (Medical Devices). The successful candidate will be responsible for ensuring compliance with regulatory standards (MDD-MDR experience is essential).
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