Responsible Technical Pharmacist

Description

Job Summary: Responsible for quality management system administration, preparation of documents for regulatory authorities, audits and process control, training, and certifications. Key Highlights: 1. Quality management system administration 2. Preparation of documents for regulatory authorities 3. Internal audits and process control Will be responsible for managing the company's entire quality management system, preparing all company quality documents in coordination with regulatory authorities, handling inspections by health surveillance agencies, preparing documents to comply with health surveillance and ANVISA requirements, understanding and applying RDC regulations for health products (RDC 665/2022), product approval and evaluation for health products, artwork development and verification, initiation and implementation of non-conformity reports, development, monitoring, and execution of Standard Operating Procedures (SOPs) for Good Practices, and delivery of SOP-related training to employees. Generation of quality-related charts, monitoring of quality indicators, classification declaration with ANVISA, product registration on the ANVISA website, development and monitoring of INMETRO certifications. Responsible for internal audits, development of standards and procedures, identification and documentation of process non-conformities, review of quality manuals and work instructions, and SOPs. Monitoring and tracking of corrective actions, audit support, documentation for regulatory and supervisory bodies such as Health Surveillance and ANVISA. Training control, planning of corrective and preventive actions, customer registration approval, supplier qualification, and monitoring of the customer service department. Employment Type: Full-time CLT Compensation: R$2\.500,00 per month Benefits: * Transportation allowance