Quality Assurance Analyst - Temporary

Description

Job Summary: A professional responsible for ensuring product quality, monitoring product releases, proposing improvements, and providing technical support in pharmaceutical manufacturing processes. Key Highlights: 1. Quality assurance and finished product monitoring 2. Technical support in resolving deviations and continuous improvement 3. Development of Master Formulas and GMP training **?****‍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\. Provide technical support to production departments in resolving quality-related technical deviations; 3\. Participate in proposing continuous process improvements; 4\. Evaluate and support production areas in complying with Good Manufacturing Practices (GMP); 5\. Develop and review Master Formulas; 6\. Support the return process of finished products from the market; 7\. Conduct training on Standard Operating Procedures (SOPs) and topics related to Good Manufacturing Practices (GMP); 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\. Participate in verifying the implementation and effectiveness of corrective actions for product- and process-related deviations; 12\. Complete the RPP checklist; 13\. Support activities related to the Administrative Assistant PL/SR; 14\. Support the Coordination team 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 at management's discretion. **?** **Requirements and Qualifications:** Bachelor’s degree in Pharmacy, with active registration at the regulatory council; Intermediate computer skills; Knowledge of quality tools and experience in pharmaceutical manufacturing and Quality Assurance routines is desirable. **?** **Additional Information:** Working hours: Monday to Friday, from 07:30 to 17:30