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The Quality Engineer will oversee quality assurance processes within the life science industry, ensuring compliance with regulatory standards and continuous improvement of systems.
This role will join an established Quality team, providing technical support on Quality and Compliance, in adherence to 13485 and MDR.
This is an excellent opportunity for an experienced Senior Accountant to join the accounting and finance team in the life science industry. Based in Cambridge, this role requires strong financial expertise to manage key responsibilities effectively.
Carry out method development and analysis of therapeutic biological products for the purposes of product characterisation and process development, supporting research and development and enabling commercial release of Biosimilars into the market.
You will manage a team to deliver analytical development aspects of specific biosimilar projects including method development for the purposes of product characterisation and process development, with the ultimate aim helping to progress projects from R&D to commercial release.
As a Lead CMC Chemist you will be responsible for supporting development, validation and regulatory submissions of APIs whilst ensuring compliance with industry and regulatory requirements. The role is a blend of hands-on chemistry, project management and supporting with regulatory submissions.
You will utilise your experience to analyse complex data sets,develop computational models, and build machine learning algorithms to support with the development of novel diagnostic platforms.
Working in R&D as a Scientist you will be supporting the team with advancing the portfolio from ideation to commercialisation. This is a lab-based role where you will be developing, optimising and executing a range of electrochemical immunoassays.
As a Technical Advisor you will be supporting customers by identifying and advising on novel solutions to challenges in the plant nutrition space. You will work to understand and identify gaps in the market, advising R&D functions on new areas of development.
As a Development Engineer you will play a key role in advancing the organisations technology. You will be responsible for developing instrumentation and test strips to support a range of activities, driving transition of the product from prototypes to pilot-scale, and ultimately full commercial launch.
This is a standalone Quality Manager role within a Business Operations team, working on business processes and ensuring compliance with ISO9001, and managing the internal audits.
The Managing Director will lead a Midlands-based medical device company, responsible for driving strategic growth, overseeing financial and operational management, and ensuring regulatory compliance. This is a hands-on leadership role, offering the opportunity to shape the future of a growing business with a global presence in the healthcare sector.
You will oversee daily operations ensuring compliance with ISO13485 & GMP regulations at all times. You will work closely with internal and external stakeholders / partners to deliver high quality production whilst driving improvements to operational efficiency and cost.
Exciting opportunity to join a market leading global animal health business.
The Client Project and Resource Manager key roles and responsibilities encompass client project initiation through to close including delegating tasks, monitoring progress, budgeting, ensuring coordination among team members and collaboration.
You will supervise the successful transfer of manufacturing processes from R&D to Manufacturing.You will be responsible for optimising the performance of manufacturing systems.
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