Job Summary: Pharmaceutical/chemical laboratory analyst responsible for conducting physicochemical analyses on raw materials and products using advanced equipment and ensuring regulatory compliance. Key Responsibilities: 1. Perform physicochemical analyses on raw materials and products. 2. Operate advanced laboratory equipment (HPLC, UV, IR, Atomic Absorption). 3. Ensure compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Job Description: **Required:** Chemist/Pharmacist/Industrial Chemist/Chemical Engineer or related degree **Experience:** 1 year in a similar role within pharmaceutical/chemical companies. **Job Objective:** Conduct physicochemical analyses on raw materials, packaging materials, intermediate products, and finished products (release testing, process testing, stability studies, and manufacturing process validation), adhering to Good Documentation Practices (GDP), Good Laboratory Practices (GLP), and ensuring that instruments and measuring equipment remain calibrated and valid; operating general laboratory equipment including HPLC, UV, Atomic Absorption, and IR. **Technical Knowledge:** * Analyze raw materials, packaging materials, intermediate products, finished products, and stability samples, and perform tests according to validated methodologies and/or pharmacopoeial methods as applicable * Operate laboratory instruments such as HPLC (High-Performance Liquid Chromatography), UV\-Vis Spectrophotometry, IR (Infrared), Atomic Absorption, among others * Interpret analytical results and prepare corresponding reports * Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results to ensure result accuracy * Interpret results and identify deviations or out-of-specification results * Prepare reagents, solutions, and calibration curves, as well as properly handle primary standards * Record results in logbooks, spreadsheets, and electronic systems * Knowledge of Good Manufacturing Practices (GMP) * Knowledge of Good Laboratory Practices (GLP) * Knowledge of Good Documentation Practices (GDP) * Current regulations (NOM\-164\-SSA1\-2015, FEUM, USP, ICH) * Analytical and problem-solving skills * Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results **Responsibilities:** Operate instruments such as HPLC (High-Performance Liquid Chromatography), UV\-Vis Spectrophotometry, IR (Infrared), and Atomic Absorption. Perform analyses on raw materials, packaging materials, intermediate products, finished products, and stability samples using volumetric, potentiometric, and spectrophotometric techniques. Ensure all analytical processes comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and current regulations (pharmacopoeias). Record, validate, and document analytical results timely and accurately, ensuring data integrity. Prepare solutions, reagents, and reference standards required for analyses, as well as perform sampling of materials. Analyze and determine root causes of results failing to meet established quality standards. **Competencies:** Data analysis Problem solving Risk management and assessment techniques Management of multiple projects Salary: $9,500\.00 \- $11,000\.00 per month Benefits: * Life insurance Work location: On-site employment