Documentation Chemist

Description

Position Summary: Responsible for managing, controlling, and ensuring the proper preparation, review, updating, and retention of documentation for the Quality Management System. Key Responsibilities: 1. Manages documentation for the Quality Management System. 2. Ensures compliance with Good Manufacturing Practices and regulatory requirements. 3. Participates in audits and operational document control. **POSITION OBJECTIVE** This position is responsible for managing, controlling, and ensuring the proper preparation, review, updating, and retention of documentation for the Quality Management System, guaranteeing compliance with Good Manufacturing Practices, regulatory guidelines, and applicable requirements of the veterinary pharmaceutical industry. **REQUIREMENTS** **Education:** Bachelor's degree in Chemistry, Pharmacy, or related field. MANDATORY. RESPONSIBILITIES * Preparation, review, and control of procedures, forms, and documentation for the Quality Management System. * Control and retention of files and technical documentation. * Administration and follow-up of change controls, CAPAs, and deviations. * Document review of manufacturing and packaging records. * Ensures compliance with GMPs and applicable regulatory guidelines. * Version control, distribution, and archiving of current documents. * Support for internal and external audits. * Follow-up on document compliance across various operational areas. SKILLS * Organizational and document control skills. * Attention to detail. * Effective communication. * Sense of urgency. * Teamwork. * Planning and follow-up. **SCHEDULE:** * Monday to Friday: 08:00 to 18:00 * Monthly rotation requiring one Saturday of work per month Employment Type: Full-time Salary: $15,000.00 per month Benefits: * Salary increases * Savings fund * Free uniforms * Grocery vouchers Work Location: On-site employment