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Demonstrated experience with Regulatory compliance and document management.
Demonstrated experience with Good Compounding Practices (GCP/BPE) and Good Manufacturing Practices (GMP).
Demonstrated experience with Deviation management and CAPA implementation.
Demonstrated experience with Regulatory audits and inspection support.
Demonstrated experience with Validation of sterile and non-sterile preparations.
View Daniel's professional profile on CazVid.
Coordinated inventory management and production requests for outsourced oncology preparations, sterile compounds, and parenteral nutrition., Performed pharmaceutical validation of oncology therapies, antibiotic regimens, and nutritional support., Conducted pharmacotherapy follow-up and adverse event analysis, supporting pharmacovigilance and antimicrobial stewardship (PROA)., Prepared consumption reports and purchasing projections for medicines and medical supplies.
Performed technical and documentary validation of chemotherapy protocols, parenteral nutrition, and magistral preparations., Conducted physical-documentary quality control and production under Good Compounding Practices (Resolution 444 of 2008)., Managed high-cost medicines, including oncology products and monoclonal antibodies.
Ensured pharmacy service operations in compliance with Resolution 3100., Implemented procedures aligned with Decree 2200 of 2005 and Resolution 1403 of 2007., Managed controlled substances and regulatory reporting., Reported adverse events through the VIGIFLOW platform.
Scheduled and supervised production of oncology preparations, sterile and non-sterile compounds, and parenteral nutrition., Ensured compliance with Good Compounding Practices and aseptic/hygiene protocols.
Ensured regulatory compliance of the pharmacy service under Resolution 3100., Supported regulatory inspections from INVIMA and the local Health Secretariat., Led the Pharmacy and Therapeutics Committee.
Reported and managed adverse events and incidents., Served as technical lead for the medical air compressor system., Managed deviations and batch release activities.