Beatriz B. Email and Phone Number

• Purchase request and stock control. As controlled reagents, and inputs for the analysis of sterile products such as eye drop and ophthalmic ointment• Collection and analysis of water and steam from all points of the factory, and cleaning validation analysis following ANVISA standards• Participating in the investigation of out-of-specification analytical results to identify the root cause and determine preventive measures to avoid its recurrence• Ensure the parameters of good… Show more • Purchase request and stock control. As controlled reagents, and inputs for the analysis of sterile products such as eye drop and ophthalmic ointment• Collection and analysis of water and steam from all points of the factory, and cleaning validation analysis following ANVISA standards• Participating in the investigation of out-of-specification analytical results to identify the root cause and determine preventive measures to avoid its recurrence• Ensure the parameters of good manufacturing practices and good laboratory practices• Physicochemical analysis for the release of products and raw materials, focusing on liquid chromatography and records of all documents, following the USP Pharmacopeia and the Brazilian Pharmacopeia Show less

• Physical-chemical analysis, focusing on liquid chromatography, and laboratory support activities• Participating in the investigation of out-of-specification analytical results to identify the root cause and determine preventive measures to avoid its recurrence• Ensure the parameters of good manufacturing practices and good laboratory practices• Inspection in the production area following the PDCA Cycle, ISO 9001 and FSSC 22000• Control the entry and exit of samples from the… Show more • Physical-chemical analysis, focusing on liquid chromatography, and laboratory support activities• Participating in the investigation of out-of-specification analytical results to identify the root cause and determine preventive measures to avoid its recurrence• Ensure the parameters of good manufacturing practices and good laboratory practices• Inspection in the production area following the PDCA Cycle, ISO 9001 and FSSC 22000• Control the entry and exit of samples from the stability chamber, according to internal procedure• Analysis of tablets and capsules, according to the stability and process validation procedure• Analysis of pharmaceutical equivalence studies performing dosing tests, related substances, dissolution, and visual and physical tests Show less

• Technical support as an analytical laboratory for field vendors, and negotiation of kit purchases with Ecolab in Saint Paul.• Preparation of solutions, analysis of finished product and raw material• Control of documents such as standard operational procedure, key performance indicator, safety data sheet for chemicals, and record of reports. Handling of customer complaints preparation of technical reports• Packaging inspection, investigation and traceability process, control of… Show more • Technical support as an analytical laboratory for field vendors, and negotiation of kit purchases with Ecolab in Saint Paul.• Preparation of solutions, analysis of finished product and raw material• Control of documents such as standard operational procedure, key performance indicator, safety data sheet for chemicals, and record of reports. Handling of customer complaints preparation of technical reports• Packaging inspection, investigation and traceability process, control of retention samples• Internal process improvement involving the areas: commercial, laboratory and logistics• 1 Month experience in the production area, following internal audit of the laboratory and production area Show less