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 and expertise to provide assay method development and validation for the quantification of drugs, metabolites and biomarkers.
Joining their dynamic and close-knit Bioanalytical team you will utilise LC-MS/MS instrumentation to undertake the quantitative analysis of a range of drugs and their metabolites within complex biological matrices, within a GLP/GCP environment.
A leading provider of laboratory services, our client delivers bioanalytical, metabolism and biomarker services using the latest analytical technology from their laboratory in York.
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.
Joining their dynamic and close-knit Bioanalytical team you will utilise LC-MS/MS instrumentation to undertake the quantitative analysis of a range of drugs and their metabolites within complex biological matrices, within a GLP/GCP environment.
A leading provider of laboratory services, our client delivers bioanalytical, metabolism and biomarker services using the latest analytical technology.
You will hold additional responsibilities in sample preparation, data processing and generating results, as well as writing and reviewing SOP's and ensuring compliance to regulatory guidelines.
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.
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 recruiting for Specialist Biomedical Scientists to join our fast paced and dynamic Microbiology team.
This role is part of a team which provides an efficient and effective Microbiology service to two general hospitals (Southend University/Basildon and Thurrock University Hospital Trusts) and local GP community.
The Role
The postholder will be expected to be able to rotate through all areas of Microbiology as required, and to perform all designated duties in accordance with local working practices.
SRG is working with a pharmaceutical company in the Northwest who require a QC manager with Biologic experience to manage and lead the QC team.
Responsibilities
Responsible for leading and managing daily activities of laboratory group to ensure compliance with quality and reliability.
Budgetary responsibility for the QC Department including management of spend and equipment capital expenditure ensuring development and testing service is provided in a cost-effective manner whilst meeting key milestone deliveries.