Posted by Hays Specialist Recruitment Limited • £80K/yr to £115K/yr
Hays Life Sciences have been exclusively retained by a VC backed biotech that has already raised tens of millions of pounds of funding and is using its novel platform technology to develop innovative medicines for areas of unmet need, allowing you to have a significant impact on patients.The company has a high-performing and innovative atmosphere, driven by the highly experienced leadership team which has an excellent track record of developing therapeutics.They are going into their next phase of growth and are looking to further build up their R&D teams within chemistry and biology with the addition of an experienced DMPK Lead to focus on leading drug discovery & development projects.This is ideally a full-time position (but could be part-time for the right candidate), with hybrid working based out of their site in London, though there is significant flexibility for remote working.
SRG are working with a Global Biopharmaceutical company to help them find a Research Associate to join their busy team.
You will be responsible for performing protein and cell-based screening assays for small molecules, biologics and new therapeutic modalities.
We are seeking a highly motivated Research Associate with experience using tissue culture and performing protein or cell-based assays, preferably in an industry setting.
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.
Global Clinical Supply Chain (CSC) is a new organization within Global Supply Chain (GSC).
GSC's vision is to be a patient-centric, integrated supply chain, launching and supplying innovative products that deliver hope to patients through life-changing medicines.
Contract Duration: 12 Months Flex to be extended/perm
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.
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.