24/04/2024 | Fulltime | Cheshire | CV-Library | £15 / Hour And timely/accurate provision of results to GLP standards. Accurate recording and analysis of laboratory data in accordance with good documentation practices Perform detailed laboratory investigations to determine the root cause of atypical and out of specification results, apply corrective and preventative
Save for laterRegister your CV24/04/2024 | Fulltime | Manchester | CV-LibraryDocumentation in accordance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines. Collaborate with quality assurance and regulatory affairs teams to support regulatory submissions and inspections. Team Leader Qualifications Demonstrated industry experience in analytical method
Save for laterRegister your CV23/04/2024 | Fulltime | England | CV-Library | £21,000 - £24,000 / Year Desirable. - Understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practice (GLP). - Technical understanding of ELISA and its applications is desirable. - Analytically/mathematically minded. - Excel skills essential. - Attention to detail and pride in work. - Works proactively both
Save for laterRegister your CV23/04/2024 | Fulltime | Huddersfield | CV-LibraryOther 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 for the department. Essential Knowledge & Experience What we need from you
Save for laterRegister your CV22/04/2024 | Fulltime | Alton | CV-LibraryProduct that has passed QC testing. The post is laboratory based and requires strict adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP) and Health and Safety Regulations. Record keeping is required into laboratory books, master documentation and onto computer databases
Save for laterRegister your CV22/04/2024 | Fulltime | Earby | CV-Library | £24,080 - £28,612 / Year Such as HPLC, LC-MS, GC-FID, GC-MS, and CETI-8. It's crucial to maintain laboratory cleanliness standards and ensure data production aligns with the Quality Management System. Additionally, you must possess relevant knowledge of good laboratory practice principles if involved in GLP regulatory studies. Hours
Save for laterRegister your CV22/04/2024 | Fulltime | Ashford | CV-LibraryFlavours by tasting Ideally basic knowledge of good laboratory practice (GLP) & safe handling of chemicals Ideally basic knowledge of good manufacturing practice (GMP) Ideally basic understanding of ISO protocols, standard operating procedures and work instructions Ability to work as an individual
Save for laterRegister your CV16/04/2024 | Fulltime | Cheshire | CV-Library | £30,000 - £45,000 / Year Their workload and planning tasks they should perform on a daily basis. Review and sign off study data. Responsible for scientific integrity and regulatory compliance of assigned studies. Ensure the data and laboratory processes are in accordance with GLP/GCP and good documentation practice. Responding to QA
Save for laterRegister your CV17/04/2024 | Fulltime | Hertfordshire | CV-Library | £25,000 / Year laboratory health and safety instructions regarding the use of personal protective clothing and equipment, and contribute to the development and improvement of safer working practices. To assist in generating risk assessments - To organise own assigned working activities. To be responsible for reporting
Save for laterRegister your CV16/04/2024 | Fulltime | England | CV-LibraryUnderstanding and application of Good Manufacturing Practices (GMP) and Good Laboratory Practice (GLP) Working knowledge of ELISA processes and workflows. Ability to be methodical, conscientious, organized and show attention to detail Ability to lead, guide direct team members in departmental procedures
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