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.
As a bioanalytical scientist, you will be primarily laboratory-based, working with the team to ensure that bioanalytical assays utilising LC-MS/MS or Ligand Binding technology are performed to a GLP/GCP standard and delivered within scheduled time frames.
The team work on a broad range of molecule types including small molecules, peptides, Oligonucleotides and Proteins.
We have an exciting opportunity for a Bioanalytical Scientist to join a fast-growing CRO based in the Cheshire area.
You will be responsible for the entire analytical process, from the preparation of biological samples such as urine and hair, to analysis using LC-MS and GC-MS instrumentation.
Primarily lab-based you will undertake a range of projects, screening for drugs of abuse in biological samples using both LC-MS and GC-MS instrumentation.
Rewarding opportunity to join a successful Drugs of Abuse testing laboratory!
Your primary responsibility will be to conduct a range of GLP/GCP regulated studies, running LC-MS/MS for pre-clinical and clinical bioanalysis and assisting with developing and validating methods.
Exciting opportunity for an experienced LC-MS Scientist to join a friendly and dynamic team, at an exciting time of expansion!
For senior candidates, you will use your exemplary communication and interpersonal skills to train and mentor junior staff members.
My client is part of a family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.
The position of Senior Analyst is within their Rapid Diagnostics laboratory located at Abingdon, UK.
Contract length: Until 31/04/2025, covering maternity leave
A QC Analyst is required by an innovative biotech company, due to unprecedented growth.
This is an integral role within the Quality Control team and would suit someone who is looking to work in a fast paced and stimulating environment, with a background in biological science and sound knowledge of good laboratory practices
Duties
Perform batch release testing of all production materials.
We are currently looking for a Microbiology Analyst to join a leading Biopharmaceutical company based in the Hertfordshire area.
As the Microbiology Assistant you will be responsible for contributing to the microbiological function of the business, by testing samples in accordance with the internal SOP's and GMP principles.
KEY DUTIES AND RESPONSIBILITIES
Your duties as the Microbiology Analyst will be varied however the key duties and responsibilities are as follows:.
The main responsibilities involve the biological safety risk assessment, by chemical analysis and characterisation, of medical devices in development.
You develop protocols, reports, and regulatory summaries in collaboration with cross-functional teams, laboratories and suppliers.
General
We are looking to recruit for a Bio-compatibility Engineer, you will be a part of the R&D team that is responsible for implementing technical strategies, evaluating and developing products, and providing a superior level of technical support.