




Position Summary: Armstrong Laboratories seeks a Process Auditor to verify and evaluate Good Manufacturing Practice (GMP) compliance in production areas through audits, ensuring product quality. Key Responsibilities: 1. Verification and evaluation of GMP compliance 2. Identification of process improvement opportunities 3. Ensuring pharmaceutical product quality Armstrong Laboratories of Mexico is seeking your talent as: PHARMACEUTICAL PROCESS AUDITOR POSITION SUMMARY: Verify and evaluate GMP compliance of documentation for processes conducted in production areas, based on current regulatory requirements, through an audit program designed to identify improvement opportunities with the aim of ensuring product quality. RESPONSIBILITIES: * Sampling of raw materials and bulk products * Line clearance in manufacturing areas * Inspection of manufacturing and packaging processes for solid, liquid, and semi-solid pharmaceutical dosage forms. * Ensure retention samples are collected during the process. * Timely sampling and routing of product during manufacturing and packaging processes. * Perform necessary physical tests according to product type and techniques. * Internal and external audits conducted in accordance with regulatory requirements. * Updating of standard operating procedures. * Process audits * ANSI table management REQUIREMENTS: * Degree in pharmaceutical sciences, biology, chemistry, or related field * One year of experience in similar positions within the pharmaceutical industry. * Knowledge of official standards WE OFFER: * Direct employment by the company * Competitive base salary * Benefits exceeding statutory requirements for permanent staff * Career development opportunities * Job stability If you are interested in this vacancy, please apply through this channel; if your profile matches the position requirements, we will contact you. "THANK YOU VERY MUCH" Salary: $16,800\.00 \- $18,500\.00 per month Workplace: On-site employment


