Fernanda Bunn Email & Phone Number

Toronto, On, Canada

• Schedule and oversee the supply and delivery of materials and products, expediting deliveries and reviewing supplier confirmations.• Evaluate MRP messages identify actions required to meet changing scheduled requirements, and take actions as placing, changing or cancelling Purchase Orders (POs).• Examine short- and long-term schedules to determine the required materials and place purchase orders.• Contribute advising Planning and other departments affected via MOC (Manufacturing Order Changes) process if unable to meet the scheduled requirements.• Ensure the materials meet specifications, quality standards, and are cost-efficient.• Help minimizing inventory levels as measured by excess, Inventory turns, Obsoletes and carrying costs by planning and adjusting POs prices, quantities and delivery dates. • Work with suppliers, customers, carriers, and internal departments, to meet and execute production plan.• Perform duties per GMP and customer requirements.

Toronto, Ontario, Canada

• Manage day-to-day Safety and Operations of warehouse;• Support Executive Team with reports, quotes and project documentation;• Assist logistics process for the development of inventory maintenance, shipments / deliveries, and returns on materials;• Keep detailed records, generate reports, and develop presentations to help management understand the logistics perspective;• Build relationships with external parties, such as suppliers, transportation companies or distributors;• Comprehend legal documents, such as contracts or import/export agreements;• Ensure cost management for supplies, transport, and warehousing;• Other associated duties as provided by Executive Team

São José Dos Campos, São Paulo, Brazil

• Quality Leader of the external manufacturer soap bar site transfer, assuring that all product and process quality was maintained during the site transfer.• Researched, developed and implemented improvements to existing processes and manufacturing systems to improve quality and productivity.• Responsible for keeping the Quality Audits, Management Review and Quality Agreement schedules for all external manufactures updated with the team. • Assured that all Change Control created at the Quality Area was completed on time.• Prepared the development of Quality Assurance documentation and controls.• Compiled and removed all external manufacturer Quality Agreements that were no longer being used.• Responsible for the development of the Risk Assessment documents whenever necessary.• Compliance with local and international audits related with External Manufacture Quality Assurance Area.

Sao Paulo, Brasil

• Took a lead role in the deviation investigation process during the production process and nonconforming products (development and release of risk analysis and research reports, follow up of action plans). • Contributed to Quality Assurance of medicine released to the market through the correct care of deviation dealing process during the production process and non-conforming products, as well as finished products released. • Executed the BRR (Batch Record Review) of all EBRs (Electronic Batch Records) of finished and intermediate products (manufacturing and packaging) identifying possible gaps as GMP standards.• Processed the batch release of finished and intermediate products in the SAP (System Application Products) system, according to analytical results of specifications, retention samples check, and EBRs approved in MES (Manufacturing Execution System), also issue of certificates of analysis of all approved finished local products. • Administered the guidelines issue of the Corporate Manual of Regulatory Local (Brazil) Rules and International Rules (FDA), through compliance of the approved procedures in the manufacturing area. • Responsible for the batch release and deviation indicators updating, as well as the actions related. • Handled the development, review and updating of Standard Operating Procedures (SOPs), and Management System Processes (PSG). • Ensured compliance with local and international audits related with Quality Assurance Area.

Sao Paulo, Brazil

• Responsible for the Manual of Good Practice of Transportation (BPT) and Standard Operating Procedures (SOP) related to all pharmaceuticals and health products along the supply chain. • GP of Transportation training of pharmaceuticals, and health products for team members. • Followed up on Regulatory Affairs legislation for pharmaceutical area. • Granted and renewed licenses and authorizations by the Sanitary Surveillance, (ANVISA - Federal Regulatory of Brazil, and VISA - Municipal Regulatory in São Paulo). • Supervised the return processes/ gathering of health, pharmaceuticals and hospital products. • Conducted the internal Quality audits and follow-up of external audits, inspections of regulatory and supervisory agencies. • Supervised the Temperature and Humidity records on fleets and transshipment areas.

Sao Paulo, Brasil

• Responsible for the Manual of Good Practice of Transportation (BPT) and Standard Operating Procedures (SOP) related to all pharmaceuticals and health products along the supply chain. • Led the Good Practice of Transportation training of pharmaceuticals, and health products for the team. • Follow up of Regulatory Affairs legislation for pharmaceutical area. • Conducted the internal Quality audits and follow-up of external audits, inspections of regulatory agencies. • Responsible for granting and renewal of licenses and authorizations by the Sanitary Surveillance (ANVISA - Federal Regulatory of Brazil, and VISA - Municipal Regulatory in São Paulo). • Supervised the return processes/ gathering of health, pharmaceuticals and hospital products. • Treatment of non-conformities and CAPA (Corrective Action, Preventive Action) plan elaboration.

Sao Jose Dos Campos, Brasil

• Checked and provided technical evaluation of medical prescriptions. • Provided pharmaceutical care to patients and prescribers. • Supervised Pharmaceutical dispensing. • Mapped and organized income and special control of prescription drugs (law 344). • Provided strong customer service: OTC (over the counter) and dispensed prescription drugs.

Post Graduate, Supply Chain Management

Post Graduation Course, Pharmaceutical Industrial Management

Graduation Course, Pharmacy