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We are seeking a Managing Director to lead a medical device manufacturing site, ensuring the delivery of high-quality, regulated products to the health care market. The role involves overseeing all functions, including production, quality, supply chain, and engineering, and commercial, while driving strategic initiatives and compliance with industry standards.
As a Legal Counsel in the life science industry, you will provide expert legal advice and support to ensure compliance and mitigate risks in the organisation. This position in Cheshire offers an opportunity to contribute to a thriving legal department within a respected company.
The Quality Engineer will oversee quality assurance processes within the life science industry, ensuring compliance with regulatory standards and continuous improvement of systems.
Our client is a leading pharmaceutical business, and they are looking to hire a high level QA Manager role. This role will take ownership of the QA teams, and provide strategic leadership.
The Operational Quality Director will take total ownership of Quality Operations at a large scale manufacturing facility on the south coast of Ireland
The QC Analyst will play a key role in ensuring the quality and compliance of pharmaceutical products and ingredients. Based in Leeds, this role involves conducting analytical testing and maintaining high standards in a laboratory setting.
Help drive the TCR engineering processes and development by leading in vivo and in vitro validation of TCEs. You'll get involved in purifying recombinant TCRs to perform high-throughput TCR display methods and deep sequencing.
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.
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