MARC for Medical Services and Scientific Research is an integrative research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.MARC is looking to have an experienced candidate for Bioequivalence Laboratory ManagerKey responsibilities:Oversee all analytical laboratory operations related to bioequivalence studies, including method development, validation, and sample analysisEnsure full compliance with GLP, GCP, and regulatory requirements during in-vitro and in-vivo study activitiesManage and supervise LC-MS/MS, HPLC, and other analytical platforms used for bioanalytical testingLead laboratory teams, assign tasks, monitor performance, and ensure proper training and competency of staffCoordinate with clinical, bioanalytical, and quality assurance teams to ensure smooth execution of bioequivalence studiesReview and approve analytical protocols, validation reports, study reports, and SOPsEnsure proper instrument calibration, maintenance, and laboratory resource managementSupport regulatory inspections and audits by maintaining data integrity and documentation complianceTroubleshoot analytical or operational issues and implement continuous improvement strategies in laboratory processesRequirementsBachelor's degree in Pharmacy or Science (mandatory)Master's degree in Analytical Chemistry (mandatory)PhD in Analytical Chemistry or related field (preferred)Strong knowledge of GLP, and regulatory compliance in bioequivalence studiesExtensive experience with bioanalytical techniques such as LC-MS/MS, HPLC, and method validationSolid understanding of both in-vitro and in-vivo bioequivalence study requirementsProven leadership and laboratory management experienceStrong skills in data review, regulatory documentation, and quality systemsExcellent problem-solving, organizational, and communication skills