Quality Assurance Analyst - Temporary

Description

Job Summary: Pharmaceutical professional focused on Quality Assurance, responsible for product release, supporting production processes, and ensuring compliance with Good Manufacturing Practices. Key Highlights: 1. Monitor finished product release based on documentation 2. Support production departments in resolving technical quality deviations 3. Participate in continuous process improvement **?****‍Responsibilities and Duties:** 1\. Perform and monitor the release of finished products to the market based on verification of production and quality control documentation; 2\. Support production departments in resolving technical quality deviations; 3\. Propose continuous process improvements; 4\. Evaluate and support production areas in complying with Good Manufacturing Practices; 5\. Develop and review Master Formulas; 6\. Support the return process of finished products from the market; 7\. Conduct training on Standard Operating Procedures and topics related to Good Manufacturing Practices; 8\. Review quality procedures and documents; 9\. Support the manufacturing process of third-party products; 10\. Participate in the approval workflow for deviations and risk analysis related to product and process deviations; 11\. Verify implementation and effectiveness of corrective actions for product and process deviations; 12\. Complete the RPP checklist; 13\. Support activities related to the Administrative Assistant PL/SR; 14\. Support Coordination in meeting performance targets; 15\. Report any anomalies encountered during task execution to the immediate supervisor; 16\. Comply with procedures related to the role and the Hipolabor Code of Conduct. 17\. Perform other similar activities as determined by the Sector Coordination, and other tasks as directed by management. **?** **Requirements and Qualifications:** Bachelor's degree in Pharmacy with active registration at the professional council; Intermediate computer skills; Desirable: knowledge of quality tools and experience in pharmaceutical manufacturing and Quality Assurance routines. **?** **Additional Information:** Working hours: Monday to Friday, 7:30 AM to 5:30 PM