Jose Luis Torres

Direct R&D and regulatory affairs activities. Keep master files; authorize changes; approve master formulas, manufacturing procedures, validation protocols, test and analysis procedures and methods, stability protocols and results, and pharmacological reviews. In charge of project management: construction, machinery and services procurement at local and international level for both company's branches (pharmaceuticals and plastics), procurement, training and maintenance of critical systems (WFI, PW, PS).

Managed Quality Assurance activities. Kept and updated Validation Master Plan, SOPs, CBAs. Imparted training on GMP and other related subjects. Drafted, revised and approved quality documents.

Managed the manufacturing and packaging operations for ophthalmic products, metered dose inhalers and effervescent vitamins. Increased total production by 15 % in units along with a decrease in rejected units percentage. Trained personnel in GMP.

Strategic Management in for the Pharmaceutical, Cosmetics, and Food Industry.

Pharmaceutical Technology / Cosmetics Technology / Pharmaceutical Sciences