
Juan J
Technical Director Quality, Compliance Food Safety
Habilidades

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Portfólio
Experiência profissional
Technical Director
Proquimes SA • Período integral
Nov 2023 - Present • 3 yrs
Currently serving as Technical Director at Proquimes S.A., a chemical manufacturing company specializing in pharmaceutical active ingredients (APIs) and food additives. Responsible for leading technical operations, quality assurance, regulatory compliance, laboratory management, and quality management systems. Key responsibilities and achievements: Leading the implementation and continuous improvement of Quality Management Systems. Coordinating SQF Food Safety Management System implementation and certification. Supporting Good Manufacturing Practices (GMP) compliance for food and pharmaceutical manufacturing. Developing and reviewing SOPs, technical procedures, quality manuals, and operational documentation. Managing quality assurance activities, laboratory operations, analytical testing, and process validation. Coordinating internal and external audits, corrective actions, and continuous improvement initiatives. Applying risk assessment methodologies, process improvement tools, and Lean Six Sigma principles. Key achievements include supporting the company's SQF certification in March 2025 and Good Manufacturing Practices certification in June 2025.
Quality Control Manager
FABRIFARMA SA • Período integral
Feb 2018 - Nov 2023 • 5 yrs 9 mos
Worked as Quality Control Manager at Fabrifarma S.A., a pharmaceutical manufacturing company, leading laboratory operations and quality control activities. Responsible for ensuring product quality, analytical reliability, compliance with Good Manufacturing Practices (GMP), and regulatory requirements. Key responsibilities and achievements: Managing quality control laboratory operations and analytical testing activities. Supervising laboratory personnel and ensuring the reliability of analytical results. Reviewing analytical reports, specifications, and quality control documentation. Ensuring compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Supporting the implementation and maintenance of quality management systems. Participating in internal and external audits, investigations, deviation management, and CAPA implementation. Coordinating continuous improvement initiatives and laboratory process optimization. Contributed to the company's Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) certification processes.