Responsible Technical Pharmacist

Description

Job Summary: Professional responsible for full management of the quality management system, preparation of documents for regulatory agencies, and audits. Key Highlights: 1. Quality management system and regulatory documentation 2. Handling ANVISA inspections and drafting standards 3. Monitoring of indicators and internal audits Will be responsible for managing the company's entire quality management system, preparing all company quality documents in coordination with regulatory agencies, handling visa during inspections, drafting documents to comply with visa and ANVISA requirements, understanding and knowledge of RDCs for health products (RDC 665/2022), approval and analysis of health products, development and verification of artwork, opening and implementing non-conformities, developing, monitoring, and executing Good Practices Standard Operating Procedures (SOPs), and training employees on SOPs. Generating quality charts, monitoring indicators, declaring establishment size to ANVISA, registering products on the ANVISA website, developing and monitoring INMETRO certifications. Responsible for internal audits, drafting standards, procedures, and process non-conformities, reviewing quality manuals and work instructions, SOPs. Monitoring and tracking corrective actions, responding to audits, preparing documentation for regulatory and supervisory bodies such as Sanitary Surveillance and ANVISA. Training control, planning corrective and preventive actions, customer registration approval, supplier qualification, and monitoring the customer service department. Employment Type: Permanent CLT Compensation: R$2\.500,00 per month Benefits: * Transportation allowance