18/03/2024 | Fulltime | York | SCIENCE RECRUITMENT UK LTDFeel and caring culture, helping to advance drug development with an excellent reputation globally. Hours of work37.5 hours per week - Monday to Friday - Flexible start times. Why join? - Opportunity to work in a modern GLP
Save for later08/03/2024 | Fulltime | England | CV-Library | £35,000 - £45,000 / Year An opportunity within a growing company in the South East as a Senior GLP Analyst has become available! As a Senior GLP Analyst you will be responsible for method development and validation of analytical methods. If you have prior analytical experience then apply below to be considered
Save for laterRegister your CV19/03/2024 | Fulltime | Merthyr Tydfil | PharmiwebAre delivered and meet regulatory requirements (GCP and GLP) and ISO 17025 (2017) standards and look to improve processes where necessary. You will also routinely assist in developing analysis methods to deliver fully validated assays and documentation of all procedures, ensuring that processes are performed
Save for later26/01/2024 | Fulltime | Gravesend | CV-Library | £15 / Hour Quality Control Laboratory Analyst GMP - GLP – Kent Opportunity Are you currently working in analytical quality control? Does your experience include hands on analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical
Save for laterRegister your CV26/01/2024 | Fulltime | Stone (Buckinghamshire), Stone | CV-Library | £15 / Hour Quality Control Laboratory Analyst GMP - GLP – Kent Opportunity Are you currently working in analytical quality control? Does your experience include hands on analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical
Save for laterRegister your CV11/01/2024 | Fulltime | Reading | VRS-UK | £35,000 - £40,000 / Year GLP Study Director to join a successful and rapidly expanding scientific laboratory within the agrochemical sector. As Study Director, you will be accountable for ensuring all studies are carried out to required GLP guidelines along with approving study data. Your responsibilities will extend
Save for later15/03/2024 | Fulltime | Cheshire | CV-LibraryQuality Assurance Auditor to join a fast-growing CRO based in the Cheshire area. As the Quality Assurance Auditor you will be required to give advice on the compliance and quality issues, and look for improvement opportunities to working practices to ensure the company's GLP and GCP regulations
Save for laterRegister your CV18/03/2024 | Fulltime | Huddersfield | CV-Library | £14 / Hour Supporting the management team by providing general secretarial and administrative services. Other tasks carried out by the support team, and which you may also assist, include providing administrative support to our ISO and GLP (Good Laboratory Practice) work, and coordinating travel and training activities
Save for laterRegister your CV15/03/2024 | Fulltime | Cheshire | CV-LibraryBioanalytical Scientist to join a fast-growing CRO based in the Cheshire area. 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
Save for laterRegister your CV15/03/2024 | Fulltime | London | CV-Library | £40,000 - £50,000 / Year In managing a team. - Experience of Pharmaceutical Regulatory Agency GMP inspections (e.g., MHRA, FDA, UKAS). QA Quality Assurance QC Quality Control MHRA FRA UKAS GMP good manufacturing practice QMS quality management system eQMS electronic quality management system Analytical testing GLP good Laboratory
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