Validation Analyst

Description

Position Summary: We are seeking a Validation Analyst with pharmaceutical industry experience to document and track manufacturing, cleaning, and equipment qualification processes. Key Responsibilities: 1. Participates in validations of processes, equipment, and analytical techniques. 2. Develops and executes qualification and validation protocols. 3. Collaborates in quality audits and annual product reviews. A pharmaceutical laboratory is seeking a Technologist, Professional, or student pursuing degrees such as Industrial Engineering, Chemistry, Pharmaceutical Chemistry, or related fields for the position of VALIDATION ANALYST. Working hours: Monday to Friday. Key responsibilities include: * Conducting, documenting, and tracking activities related to manufacturing process validations, cleaning process validations, equipment qualifications, analytical technique validations, critical support system validations, computerized system validations, and spreadsheet validations. * Developing and executing qualification and validation protocols outlined in the Validation Master Plan. * Preparing protocols and reports for equipment, process, system, and analytical technique qualifications and validations. * Organizing and planning daily work using necessary resources in accordance with the Validation Master Plan. * Developing and reviewing analytical procedures. * Participating in internal and external quality audit teams. * Actively participating in data collection and analysis within the "Annual Product Review" system to evaluate trends in product parameters or variables. * Participating in Validation Committee meetings to address relevant topics. * Interacting with production, maintenance, quality control, and technical management personnel to perform assigned duties. * Tracking calibration of instruments used in process qualification and validation. * Participating in process standardization. And other duties inherent to the position. Employment Type: Full-time Work Location: On-site