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4.0 - 8.0 years

0 Lacs

karnataka

On-site

As a diligent and detail-oriented Laboratory Supervisor, you will be responsible for overseeing the workflow to ensure optimal efficiency in testing processes and timely delivery of results. Your duties will include verifying quality control measures, such as validation of new reagents and other quality assurance activities, to uphold the performance of tests. It will be your responsibility to review and maintain records of test results and data archives, and ensure adherence to Infection Prevention and Control (IPC) procedures in the work environment. Your role will also involve evaluating proficiency testing and approving records, as well as reviewing and signing off on departmental standard operating procedures for clinical assays. Providing advisory services to patients, customers, and consultants on tests when necessary is a key aspect of this position. Participation in management review meetings, internal audits, and offering insights for continual improvement will be expected. You will be required to follow laboratory policies and procedures diligently, including proper attendance and time reporting. Additionally, managing mail communications of abnormal results and coordinating with public health departments or regulatory bodies will be within your purview. Ensuring that technicians comply with proper Bio-Medical Waste (BMW) management protocols, editing results as needed after retesting, and serving as a technical resource through staff training and participation in educational opportunities are essential responsibilities. You will be tasked with evaluating employees" competencies and providing guidance on the verification and implementation of new tests, kits, and instruments. Testing the virulence and strength of specific microbes to develop improved diagnostic and treatment methods, planning and organizing resources and activities, maintaining accurate records, and staying updated on new research findings and industry events are vital components of your role. Collaborating with colleagues from various departments, offering advice to medical staff and external bodies, and implementing preventive measures to curb the spread of infections in the laboratory are also part of your remit. Participating in quality improvement initiatives, reviewing critical values, interpreting and authorizing reports in Hematology and Clinical Pathology, and assisting in the recruitment of consultants as per approved requirements will be among your responsibilities. This is a full-time position that requires a minimum of 4 years of experience in Hematology. The work location is on-site, and your dedication and expertise will contribute significantly to the success of our laboratory operations.,

Posted 3 days ago

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