Daniel Porto

Management of all operations employees (approx. 120 employees). Responsible for production process review, kpi´s, quality requirement achievements. Top management representative in all external audits (GMP, ISO 9001, ISO 13485 and products CE mark). Internal Auditor for QMS (ISO 19011, 9001, 17025). Main responsible for production crew training on GMP, ISO 13485 MDD and clean room requirements. Lean Six Sigma Black Belt in continuous improvement projects.

- Supervision of 3 medical devices production areas and Supply Chain. - Work In Progress System implementation. - Internal auditor.

Management of Industrial Activities (manufacturing, planning, QC and QA), Contracts and Regulatory Affairs Manager, GMP and Validation Master Plan Coordination, Supply Chain supervision, Lead Auditor (internal and external). Development of 2 industrial arquitectural projects aiming GMP. Top management representative with all regulatory Body of Knowledge. Key user in MRP systems implementation.

Quality Control of raw materials, intermediate products and finished pharmaceutical products. Development of material specifications to meet pharmacopoeia parameters and technical reports of registered products. Writing of standard operational procedures and documents related to GMP guidelines. Team training aiming at the implementation of GMP.

MBA focused on Manufacturing and Quality Tools, resources and project management and industrial costs.

Pharmaceutical Technology.