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Are you a Life Sciences Professional relocating to the UK in the next few months? Michael Page Life Sciences recruit across the full drug life cycle from discovery to patient delivery, focusing on entry level to C-suite roles. We work with pharmaceutical, biotech, biopharma, and medical device companies, as well as CROs and consultancies across the UK.
I'm currently looking for a Quality Specialist based in Gloucestershire, this position requires someone with experience in a QA/QC position within labs, and experience working to ISO17025.
You will be responsible for development and validation of a number of assays with focus on virology techniques. You will be working on a range of bespoke R&D project, helping to deliver innovate clinical research.
As a part of the regulatory team you will be responsible for obtaining and maintaining generic and branded marketing authorisations for designated EU and non-EU territories (through internal and Third Party workstreams) to ensure on-time launches, continued supply and the compliance of all products. This roll will also provide the opportunity to develop management skills within the team.
As a Principal Scientist with focus on analytical chemistry you will provide SME support with analytical testing, scientific consulting and regulatory support to help key customers advance key products into the market!
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
The Integrity & Compliance Manager/Associate Director will be responsible for supporting, managing and enhancing Most of World (MoW) implementation of the Global Integrity & Compliance Program (HCC focus).Establishing clear policies and offering pragmatic, solutions-orientated guidance and program support to the AUA Integrity & Compliance Officer.
As a QA Auditor within the QA team you will plan and conduct audits of processes, systems, facilities, studies and documents to ensure compliance with GCP. You will play a vital role in ensuring general compliance and effectiveness of the CRO.
Providing support within the regulatory function maintaining and expanding the specified product registrations within UK and EU.
You will support with building AI models to aid discovery of novel cancer-cell receptors using knowledge of protein structures and sequences, which can then be validated to support with creating novel therapies.
The purpose of this role is to make sure that the labelling is updated and compliant and meets the necessary trademark deadlines.
Excellent opportunity for an advisory role for Healthcare & Life Sciences (Medical Device/ Diagnostics/ Biotech)
As a highly driven Senior Scientist, you will be supporting the R&D Team in the development and optimisation of novel diagnostic assays.
You will be instrumental in delivery of analytical activities across a portfolio of new respiratory products, successfully leading projects as they progress into clinical studies and through to commercialisation!
As a Senior Manager (Analytical Team) you will lead on delivery of all analytical activities taking new products through to clinical studies and subsequently commercialisation. The main focus of research is respiratory treatments.
The client are a developing biotech undergoing expansion, with the aim to support in development of novel t-cell therapies.
You will utilise existing knowledge and a variety of research methods relating to cell line engineering, molecular techniques and screening assays to support development of novel t-cell therapies.
Our client is an expanding MNC with focus in Hong Kong and China markets currently.
Lab Operations Manager role in a sizable team in Biotech Company with focus on medical/ healthcare research and drug development.
As a Study Operations Manager you will be responsible for coordinating and overseeing delivery of a number of clinical studies from an organisational point of view. You will directly manage a team of Senior Scientists to deliver.
As a Principal Scientist you will be an SME in your area supporting, advising and overseeing a number of specified clinical studies. You will perform a key role in the development of scientific operational staff.
As a part of the regulatory team you will provide UK national support for new product MR/DC or CP submissions managed by CRA teams and provide support to other UKRA team members as required and assist other UKRA team members to produce documentation and submissions.
Working in the Project Management team as project owner, assisting with technical and commercial aspects. Running projects in a controlled and timely manner, utilising project management methodologies and planning in accordance with multi-site processes.
Research Assistant to contribute to the development of hydrogel drug delivery systems for the oral administration of small molecules and biologics.
Play a vital role in helping pharmaceutical and life sciences companies navigate the complexities of market access for their innovative products. Contribute to optimizing product reimbursement, formulary placement, and successful market entry, ensuring that patients can access the treatments they need. This position offers a unique blend of strategic thinking, data analysis, and collaborative problem-solving within a supportive and innovative environment.
Responsible for life cycle management relating to variation submissions, renewals, labelling updates and preparing dossiers to meet national submission requirements. You will also be maintaining national aspects of Global Regulatory Systems.
Maintaining a focus on the value of patient-centric outcomes whilst ensuring that clinical programs have a innovative PRO/COA Strategy. Defining and overseeing the execution of strategies and guiding the development and validation of instruments in clinical trials and studies.
To effectively aid in ensuring validation studies and activities are planned and executed in line with defined external and internal standards. The main focus of the role will be process validation, equipment qualification and cleaning validation.
Working with the editing team to help manage and maintain professional scientific standards.As part of the publishing team, you will act as liaison between all internal and external parties.
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