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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.
An ideal role for someone experienced within QA/QC roles working to ISO17025
As a Director of Medical Affairs, you will provide leadership within the Medical team, driving strategic initiatives and managing a dedicated team. The role requires a charismatic forward thinker, responsible for UK launch of new exciting products.
The head of Quality and Regulatory must lead the quality and regulatory agenda ensuring customer and regulatory requirements are met.Also the succesful applicant will need to develop Quality culture, and ensure that all staff within the business are operating to the highest level of compliance.
This is an exciting opportunity to join as an Operations Manager, where you would be orchestrating internal operations, during a period of growth and innovation for the business. The successful candidate will be working alongside the founders, being at the heart of their administrative effectiveness, taking charge of key operations.
This role will have full oversight of the EU and Ireland Quality function as this business develops into Europe. Currently this business has only a handful of employees in Europe, therefore the successful applicant will be tasked with aligning EU Quality with the global Quality vision as operations develop.
This role is vital to the UK operations of this client, as a standalone Quality role. The main focus areas of this role are QMS/eQMS and RP/RPi duties.
As a Senior Firearms Scientist, you will utilise your knowledge of firearms examination and forensic analysis to contribute to a highly skilled Life Sciences team. Based in Wantage, this role provides an excellent opportunity to apply your skills in a business services environment.
We are currently looking for a Reporting Forensic Scientist to join a dynamic and thriving Fingerprint Recovery team. Based in Oxford, successful candidates must have experience working within a Forensic environment.
This is a prestigious opportunity for a VP/SVP of Partnerships to play a pivotal role in a leading Life Science company. The successful candidate will spearhead collaborations, develop strategic partnerships, and champion growth initiatives across the US with flexible working out of the HQ in San Francisco.
This is an exciting opportunity to join an early-stage biotechnology startup as a Research Associate where your drive and expertise will spearhead the refinement of their TCR engineering processes. You'll play a crucial role in curating datasets to inform their AI algorithms, affirming their platform's efficacy, and identifying TCRs.
You will utilise specialist knowledge relating to cell culture techniques and GMP standards to support with developing manufacturing processes for novel clinical trials in the CGT space
Our client is an expanding MNC with focus in Hong Kong and China markets currently.
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 detail-oriented Labelling Specialist / 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.
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).
Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.
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