Monitor product manufacturing in a way that result in company compliance with regulatory SOP, GMP, HACCP, standards for third party audit and customer product requirements. Perform HACCP and SSOP validations and verifications. Execute of training programs that support the company’s objectives regarding quality and food safety. Oversee company’s pest control program. Assist on customer complaint investigations. Ensure sanitation requirements are maintained in all areas of the facility. Work with management as needed to reduce complaints and implement appropriate corrective actions.

• Inspection and analyses of products for safety, product quality, and packaging quality.• Training and follow up inspections to line workers for GMP compliance.• Prepare documentation of quality inspections and results throughout the manufacturing process.• Oversee and monitoring sanitation, safety regulations and procedures for GMPs and HACCP compliance.

Investigation of possible pharmaceutical combinations for developing new products.Leader of the project Tramadol/Celecoxib, responsible for organizing and performing activities regarding the selection of API's supplier, purchase of API, collaboration with the formulation team, analysis of raw material, development of analytical methodoly for analysis of finished product, manufacturing of trial batches, preparation of CTD dossier for submission to regulatory authorities.Preparation of protocols, reports and documentation regarding manufacturing processes and quality control.Handling of deviations, root cause analysis, 5 whys analysis and CAPA system.Developing of risk assessment regarding changes in establised procedures.Application of 5S guidelines in laboratory to increase work efficiency.Coordination of calibration and qualification activities of equipment in laboratory.Organizing and performing of Kaizen activities in the laboratory.Experience working in a quality environment under cGXP, USP, ICH, FDA, EU guidelines complying USA and European standards.Experience in internal and external audits for EMA, INVIMA and ANVISA certifications.

Validation of analytical methodology for quantification and dissolution analyses of finished product under ICH and cGXP guidelines and complying with USA and European standards.Generate protocols and reports of validation and method transfer using CTD format.Generate and update SOPs.Collaboration with validation of manufacturing processes and cleaning validations.Handling of deviations, root cause analysis, 5 whys analysis and CAPA system.Development of risk assessment regarding changes in established procedures or methodologies.Investigation and reporting of OOSs.Application of 5S guidelines in laboratory to increase work efficiency.Coordination of calibration and qualification activities of equipment in laboratory.Organizing and performing of Kaizen activities in the laboratory.Experience working in a quality environment under cGXP, USP, ICH, FDA, EU guidelines complying USA and European standards.Experience in internal and external audits for EMA, INVIMA and ANVISA certifications.

Performing of laboratory tests including toxicology, chemistry, hematology, immunology, and microbiology; receiving, typing, testing, and recording blood bank inventories.

Performing of laboratory tests including chemistry, hematology and immunology. Implementation of quality management system.

Performing of laboratory tests including chemistry, hematology and immunology.

Supply medicines to patients, whether on prescription or over the counter. Provide information to patients and other healthcare professionals. Inventory control.