Cindy Saenz Email & Phone Number

Sydney, New South Wales, Australia

• Conducting tests on raw materials, in-process components, intermediate and finished products to ensure they meet quality standards.
• Analyzing quality data to identify trends, patterns, and potential areas for improvement.
• Monitoring and managing laboratory supplies, reagents, and equipment.
• Used SAP software for incoming material control, entering QC data and generating required documentation.
• Trained and coached existing and new employees on new testing methods, equipment operation, and safety procedures.
• Participating in continuous improvement initiatives to enhance laboratory processes, efficiency, and overall quality control measures.

Bogotá D.C. Area, Colombia

• Knowledge in aerobic and anaerobic wastewater treatment plants and contaminated soil.
• Improved and optimised Wastewater Treatment Plants for food, beverage, pharma, chemical and petroleum industries using bioremediation treatments.
• Managed and control of company's technical documentation according to Good Documentation Practices (GDocP).
• Ensured that quality of water, treatment and supply of product comply with quality regulations for disposal of wastewater and underground water to city's sewage source or natural sources such as rivers or sea.
• Determined corrective actions for maintenance when equipment failed or required repairs
• Monitored KPIs to proactively address bottlenecks and quality issues.

Bogotá D.C. Area, Colombia

• Reviewed and analyzed raw materials of pharmaceutical products according to schedule of priorities.
• Managed analytical (physical and chemical) testing of raw materials, in-process samples utilizing titration, UV-Vis, FTIR, and other instruments.
• Operated Procedures (SOPs) and current Good Manufacturing Practices (cGMP) to promote safe working environment.
• Participated in continuous improvement by generating suggestions, engaging in problem-solving activities to support teamwork.
• Performed routine maintenance and calibration on testing equipment.

Bogotá D.C. Area, Colombia

• Updated specifications and analytical methods of finished products and raw material either by changes such as monographs of pharmacopoeias (USP/ BP), reformulations of products, sanitary registration, tests and.
• Performed duties in accordance with work procedures, Standard Operating Procedures (SOPs), Good Documentation Practices (GDocP) in pharmaceutical and current Good Manufacturing Practices (cGMP)
• Maintained document templates for controlled documents.

Advanced Diploma, Leadership Management

Advance Diploma, Project Management

Diploma, Project Management

Certificate Iv, Project Management

Course, English

Course, Auditor In Iso 9001:2005; Iso 14001:2005 And Ohsas 18001:2007

Course, Safe Handling Of Chemical Substances

Course, Enviromental Management System Sga Standard Ntc Iso 14001

Chemical Engineering