Life Sciences jobs in England

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.

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 Laboratory Technician, you will play a pivotal role in supporting the department's research endeavours by assisting in the execution of experiments, maintaining laboratory equipment and stocks, and preparing growth media. This role offers a unique opportunity to contribute to groundbreaking scientific discoveries that have a direct impact on the advancement of medical knowledge and patient care.

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

You will conduct relevant surveys and provide specialist advice from an Ecological point of view, helping embed the approach from the very beginning of new projects.

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.

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.

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.

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.

I'm currently looking for a Quality Coordinator based in Gloucestershire, this position requires someone with experience in a QA/QC position within labs, and experience working to ISO17025.

Exciting opportunity for an experienced regulatory lawyer to join a global animal health company on their general legal team, working from Liverpool. A competitive salary is on offer.

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.

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.

Responsible for providing technical support to the Toxicology team working alongside the Head of R&D, Method Development & Quality. Proficient, to a legally defensible standard, in techniques such as immunoassay, LLE, SLE, and liquid chromatography-mass spectrometry.

You will provide technical expertise and project management across bioanalytical activities, including oversight of outsourced bioanalysis at CROs for both clinical and pre-clinical drug development.

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 Senior Research Scientist in the clinical trial space, you will be leading the analytical stage of clinical trials and acting as a technical Subject Matter Expert (SME) in the scientific discipline.

As a Clinical Research Associate, you'll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs and medical devices experts to identify, select, initiate and close-out investigational sites for pre and post market studies, ensuring adherence to applicable regulations and principles of ICH-GCP.

As a Senior Proposal Manager you will be responsible for managing all aspects of proposals, monitoring and overseeing the scope of work and budgeting process to generate accurate and timely proposals.

Manage and coordinate all laboratory operations, including sample processing, data analysis, and quality control procedures. Oversee the allocation of resources, ensuring optimal utilization of equipment, supplies, and personnel.

As an SDS Specialist / Hazard Comms professional you will primarily focus on working within the EU market to provide technical scientific input into SDS generation / updates.