Analytical Development Chemist C

Description

Job Summary: Responsible for raw material analysis, input analysis, finished product analysis, analytical method validation, drug characterization, and dissolution profile development. Key Highlights: 1. Participation in DOSSIER compilation 2. Development of validation and method transfer protocols 3. Knowledge of pharmaceutical regulations (NOM-059), ICH guidelines, SUPAC, FDA Responsibilities \* Perform raw material, input, and finished product analysis \* Analytical method validation \* Participation in DOSSIER compilation \* Development of validation and method transfer protocols \* Issuance of analytical methods \* Characterization of reference drugs \* Conducting dissolution method profiles Social or Economic Benefits We are the pharmaceutical company with the best incentive program for new product development. \* In addition to salary, project participants receive a bonus for each developed product. Other Requirements Knowledge of regulations applicable to the pharmaceutical industry (NOM\-059\), ICH guidelines, SUPAC, FDA, and familiarity with FEUM and USP. Bachelor's degree in Pharmaceutical Chemistry and Biology (QFB), Chemical Engineering, or related chemistry field; degree completed and professional license obtained