Pharmaceutical Technology Development Analyst

Description

Job Summary: Pharmaceutical Technology Development Analyst for New Products, responsible for preparing reports, formulating laboratory batches, and overseeing manufacturing to ensure quality in the pharmaceutical industry. Key Highlights: 1. Focus on pharmaceutical technology development of new products. 2. Involved in preparation and review of reports and formulations. 3. Full oversight of product manufacturing. **Pharmaceutical Technology Development Analyst Position \- New Products** **Work Location:** Hipolabor Unit I \- BR 381 Highway Km 12.3, Borges – Sabará – MG ZIP Code: 34735\-010 **Working Hours:** 7:00 AM to 4:48 PM, Monday to Friday **Education:** Bachelor's degree in Pharmacy **Language Requirement:** Basic English **Experience Required:** Familiarity with pharmaceutical industry routines. Pharmaceutical technology development knowledge (preferred). **Microsoft Tools Proficiency:** Basic Office suite. **Job Responsibilities:** 1\. Prepare/review Pharmaceutical Technology Development Reports related to New Products. 2\. Prepare/review Initial History Reports for New Products. 3\. Prepare Production Technical Sheets for Laboratory Batches and Placebos related to New Products and request their manufacturing. 4\. Prepare Laboratory Batches and Placebos related to New Products and perform primary stability testing. 5\. Provide Laboratory Batches, Placebos, and Pilot Batches to requesting departments. 6\. Prepare/review Pilot Master Formulas and Initial Release Formulas related to new products and collect signatures from responsible personnel. 7\. Monitor the Weekly Production Scheduling Records for Production Lines at Hipolabor Units I and III. 8\. Provide Production Technical Sheets for Laboratory Batches and Pilot Batches to SPCP, including calculations of Active Pharmaceutical Ingredient (API) assay and moisture content. 9\. Monitor manufacturing of Laboratory Batches, Pilot Batches, and Industrial Batches related to New Products at Units I and III, and prepare Manufacturing Follow-up Reports. 10\. Evaluate suppliers of raw materials related to new products, as designated by the Systemic Quality Assurance Department, based on pre-formulation test results, laboratory batches, placebos, pilot batches, and industrial batches. 11\. Monitor deviations, non-conformities, RTs, and RCMs. 12\. Monitor manufacturing stages of outsourced products related to new product development. 13\. Prepare/review Risk Assessments. 14\. Perform document reviews within deadlines, ensure compliance with standard operating procedures and Good Manufacturing Practices, and report any non-conformities to supervisors. 15\. Monitor the first Industrial Batches of products. 16\. Conduct training on quality documents.