Pharmaceutical Analyst - Analytical Development

Description

Job Summary: Professional to develop and validate analytical methods, ensuring regulatory compliance and proper equipment operation. Key Highlights: 1. Experience with liquid and gas chromatography (HPLC, UPLC, GC) 2. Knowledge of regulatory guidelines and applied statistics 3. Preparation of technical reports in English and Portuguese Description: Apply quickly via email: Requirements and Qualifications: * Bachelor's degree completed in Pharmacy, Chemistry, Biomedicine, Chemical Engineering, or related fields; * Experience with liquid and gas chromatography (HPLC, UPLC, GC); * Knowledge of UV-Vis and IR spectroscopy, dissolution testing, and classical quantification techniques; * Familiarity with regulatory guidelines (RDC 166/2017, RDC 318/2019, RDC 964/2025, ICH Q2, Q3, Q6, USP, and ); * Basic understanding of applied statistics for validation (DPR, ANOVA, linear regression, robustness, variability); * Ability to prepare technical reports in English and Portuguese. Desirable: * Prior experience in an Analytical Development environment; * Practical knowledge of maintenance and calibration of analytical equipment; * Experience with audits and regulatory inspections; * Intermediate or advanced English proficiency. Responsibilities and Duties: * Development and validation of analytical methods according to current regulations and defined timelines; * Comprehensive and accurate technical reports, compliant with regulatory requirements; * Analytical equipment fully operational, ensuring result reliability; * Adherence to project deadlines and regulatory demands; * Active contribution to maintaining Good Laboratory Practices (GLP) and the Quality Management System. Working Hours: Weekly workload: 44 hours Knowledge: Education: Bachelor's degree \- Biomedicine, Chemical Engineering, Pharmacy, Chemistry \- Completed 2511080202181856592