1 to 7 of 7 Permanent GLP Jobs in Yorkshire

made correctly Write reports on the analysis carried out for CofAs. Ensure that the testing done is carried out to the required standard (GMP, GLP, MHRA etc). What do you need to be considered? You will need: Degree or equivalent experience in science-based subject, ideally Chemistry. Working knowledge … of analysing organic compounds such as fine chemicals, petrochemicals, or APIs. Knowledge of working in a regulated laboratory and standards such as UKAS, GMP, GLP, MHRA, FDA etc. What to do next? Interested? Of course you are, who wouldnt want to work for a great company with a supportive team more »

Are you already working in a GLP/GCP environment and want to consider Quality Assurance as your next career move? Do you want to be part of a company that helps build a healthier and safer world? Are you looking for industry recognised training and development opportunities? Labcorp is … a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. As a GLP Quality Assurance Auditor at Labcorp based in Harrogate, North Yorkshire , you will play an essential part in making this happen. We are looking for someone who is able to apply … preferred (or equivalent Life Science experience) Experience may be substituted for education Skills/Experience: Proven work history in a regulatory environment working to GLP/GCP Ability to apply basic relevant regulatory knowledge Ability to follow instruction e.g. QA documents (SOPs) Ability to assimilate/interpret operational documents such more »

health and safety procedures and guidelines. Education and experience: - Degree education in Chemistry, Chemical Engineering or other related Engineering discipline. - Knowledge of GLP (Good Laboratory Practice) quality requirements skills gained in similar work (or dissimilar but relevantly skilled work). - Awareness of REACH, CLP, ISO 21469, NSF, AS9100. - Awareness of more »

molecule bioanalytical studies. 3. A working knowledge and practical experience using LC-MS/MS. Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified more »

within the Bioanalytical Services –Small Molecules group. You will be responsible for delivering high quality results to our Sponsors and Clients in compliance with GLP and GCP. WHAT WE OFFER: Auto Enrolment Pension Comprehensive Benefits Package Working within a Global organisation Career Advancement Opportunities including Apprenticeships KEY RESPONSIBILITIES: Quality: Follow … knowledge of large molecule analysis in support of PK and PD studies. Experience working in a regulatory environment, managing studies that are compliant with GLP/GCP Experience in a client facing role with the ability to provide high level advice and guidance to clients Non-Smoker: due to the more »

Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC Experience Responsibilities more »

Salary and Benefits of QC Analyst Salary up to £27,000 Permanent Role Skills and Qualifications needed for QC Analyst Awareness of GMP/GLP Standards Pharmaceutical or Chemistry Degree 2 Years Experience in a relevant role Fine Chemistry/Pharmaceutical Experience 2 years of HPLC and GC Experience Responsibilities more »