This experienced QC Laboratory Manager has over 13 years of experience in GMP-regulated environments, currently he is a QC Manager and Trainee Qualified Person (QP) managing a team of analysts, scientists, and senior analysts where he’s responsible for factors like budget management, resources, and staff development.
He has a deep experience of HPLC, GC, UV-Vis, and Karl Fischer including validation (IQ/OQ/PQ), stability testing protocols, and cleaning validation. He has got the background in MHRA and FDA standards, as well as experience with ISO and GLP and Quality Management Systems.
He is experienced in in audit readiness and has participated in audits as a Subject Matter Expert (SME) aligns so will be able to assume duties as the process owner for quality standards. He has been working in managing quality management systems, Deviations, CAPAs, and OOS/OOT investigations using root-cause analysis.
Finally, he’s got experience in approving finished goods and supporting the release process prior to QP certification so could potentially assume the Release Authority duties. He is on a path toward QP qualification, with a strong technical and regulatory skill set to bring to the role. He has lived in the North West and South East before. He is available due to redundancy in his company and can relocate on 1 months notice. To enquire please email admin@licasci.com quoting ref 11929