Job Summary: Responsible for ensuring technical and scientific excellence in laboratory processes, coordinating teams, and promoting professional development. Key Highlights: 1. Ensure technical and scientific excellence in laboratory processes 2. Coordinate teams and develop staff members 3. Ensure regulatory compliance and humanized patient care **Job Description:** Ensure technical and scientific excellence in laboratory processes, guaranteeing the quality of clinical analyses, regulatory compliance, and standardization of services provided. Act in a humanized and solution-oriented manner in supervising Collection Units, coordinating teams, promoting staff development, and ensuring differentiated care aligned with patients’ specific needs, in accordance with Laboratório De Vita’s mission and values. **Job Requirements:** * Completed undergraduate degree in Biomedicine, Pharmacy, Biology, or related fields; * Active and valid professional council registration (**CRBM, CRF, or CRBio**); * Legal qualification to assume Technical Responsibility; For Biology graduates with a teaching degree — Postgraduate specialization in Health: Clinical Analyses, Hematology, Microbiology, Biochemistry, or Laboratory Management (mandatory) **Responsibilities:** * Collect biological samples from patients, ensuring appropriate and humanized reception. * Properly prepare and identify samples, ensuring traceability and correct handling, processing, and storage of biological samples. * Inspect biological material for analysis, verifying compatibility and condition against established criteria. * Perform analyses efficiently and effectively, maintaining necessary records to ensure result accuracy and consistency; correlate findings with complementary patient data and remain vigilant regarding critical or discrepant values. * Operate clinical analysis equipment, understanding its functionality—including possible "flags"—and perform calibration, verification, and maintenance through daily, weekly, and monthly controls, recording all activities in dedicated spreadsheets focused on damage prevention. * Conduct internal and external quality controls, critically analyze results, and report them on designated platforms. * Enter results into Laboratory Information Systems (LIS), ensuring accuracy. * Strictly comply with biosafety and occupational safety regulations. * Support preventive and corrective equipment maintenance as needed. * Collaborate in internal and external audit processes. * Maintain departmental organization, overseeing supplies, materials, and the work environment. * Dispose of biological material according to established timelines and biosafety standards. * Know instructions for all analytical processes involved in test execution. * Supervise document control for the assigned Unit, including SOPs, forms, maintenance logs, temperature monitoring records, and mandatory legal documents. * Assist in drafting and reviewing area-specific documents. * Request equipment maintenance, repairs, and replacements as needed, maintaining proper records. * Supervise and guide technicians and assistants in their duties. * Monitor and implement internal and external quality control programs. * Review, release, and sign test reports when authorized. * Ensure adherence to biosafety standards and technical protocols. * Participate in internal and external audits, providing technical evidence. * Conduct training sessions for technicians or assistants as required, evaluating efficiency and effectiveness throughout the process. * Research, propose, and implement technological and scientific innovations in the laboratory. * Assist in clarifying technical questions raised by technicians, assistants, or front-desk staff as needed. * Record and communicate critical results, and notify municipal health authorities of suspected or confirmed notifiable diseases. * Monitor updates to laws and regulations applicable to the laboratory sector and promote adaptation to potential changes. * Provide technical support to physicians and patients upon request. * Monitor, accompany, and support visits by regulatory agencies (e.g., Sanitary Surveillance, Professional Councils, and other competent entities), ensuring laboratory processes comply with current legislation. Act as the institution’s technical representative during inspections, providing clarifications, presenting evidence, and coordinating implementation of any requested adjustments.
João Silva
Indeed · HR
João Silva
Indeed · HR
