Partnering with customers across the bioanalytical sector working to optimise programs during the crucial stage of the drug discovery and development process, they give technical insight, expertise and flexibility to provide assay method development and validation for the quantification of drugs, metabolites and biomarkers.
Joining the business as an integral member of the team, you will act as Study Manager for a range of regulated and non-regulated small molecule bioanalytical projects, ensuring these are conducted in compliance with regulatory standards, and are on time and within budget.
A leading provider of laboratory services to global clinical trials, our client delivers bioanalytical and toxicology programmes from their state-of-the art facility in York.
You will be involved in the whole process, from sample preparation, through to data analysis, assisting in developing and validation of methods where required.
Your primary responsibility will be to conduct a range of GLP/GCP regulated studies, running LC-MS/MS for pre-clinical and clinical bioanalysis projects.
Exciting opportunity for an experienced LC-MS Scientist to join a friendly and dynamic team.
Posted by Hays Specialist Recruitment Limited • £53K/yr to £67K/yr
You will be joining a global leader in the medical diagnostics field who are looking for someone to join their expanding insights & analytics team and help provide in-depth analysis, support and strategy suggestions to multiple parts of the business.
The company has a fantastic corporate culture and is highly driven by making a real impact/difference to patients.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a contract basis.
The duration of the contract will be 23 months with a start date in September 2024.
A unique opportunity has arisen for a Laboratory Scientist to make a move into a more data focused role with a leading bioanalytical CRO in Macclesfield!
Joining a dynamic team, you'll will be utilising your analytical and problem-solving skills to check scientific data and calculations.
You'll be supporting study directors and projects leaders in data analysis ensuring all data is in compliance with regulatory standards, aiding with the timely delivery of projects to clients.
We are currently seeking an experienced Analytical Chemist to join our client's dynamic team in Cambridgeshire.
The ideal candidate will possess a robust knowledge of analytical chemistry and hands-on experience with instrumentation such as HPLC (essential) and Mass Spec.
This role is crucial for ensuring the quality, safety, and sustainability of pharmaceutical products, and requires a detail-oriented individual who can document technical procedures and summarise data with minimal supervision.
Develop bespoke, complex ligand binding assays/immunoassays to successfully quantify biomarkers and gene therapy targets found in biofluids & tissues samples.
Optimise experimental design, troubleshoot technical issues & provide expertise in assay progression from R&D to clinical development phases.
General
Career defining opportunity to join a prestigious Biopharmaceutical organisation as a Research Scientist