Drug Development Solutions Jobs in United Kingdom

+We're looking for a Document Quality Associate to join the team. · +The role will focus on QC checking reports to a high standard, taking into account report amendments, deviations, investigations and all relevant SOPs and working practices. · ...

The Senior Scientist Forensic Analyst will lead and perform sampling, analysis, and identification of contamination using light microscopy, chemical tests, FTIR, · and SEM/EDX. · ...

+To manage the effective delivery of the UK HR service across the business, covering all aspects of the employment life cycle, including but not limited to employee relations, learning and development, wellbeing, talent acquisition, payroll and benefits and overseeing the HR admi ...

The candidate will carry out testing on pharmaceutical samples throughout the pharmaceutical program lifecycle using various tools such as Powder X-Ray Diffraction (PXRD), Thermal analysis, Scanning Electron Microscopy (SEM), or sorption techniques. · ...

The ideal candidate will; be enthusiastic proactive driven to go the extra mile to support our customers focus on quality possess an excellent attention to detail communicate effectively be flexible productive realise that timelines priorities requirements will change regularly r ...

Build strong partnerships with our customers to help them progress their drug development pipeline. · ...

The Document Quality Associate will be responsible for performing regulated studies to the appropriate GLP/GCP standards and latest regulatory guidelines. · ...

The Sample Management team is responsible for delivering a range of services to our bioanalysis laboratories on site at Fordham, working to GxP regulations. · Prepare sample batches for analysisPerform QC checks for returned batchesReceive and log in samplesUse of LIMS system to ...

The CSV Engineer will be responsible for validating computerized systems in accordance with regulatory requirements and company policies. · Validate computerized systems in accordance with 21 CFR Part 11. · Support CSV activities of the Quality Management System including deviati ...

A member of the Analytical Sciences team involved in and taking responsibility for all aspects of analysis using LC-MS GC-MS and ICP-MS. · ...