PHYLLIS OKONMAH

• Performed GMP Inspections,recorded findings and collaborated with quality/production/Maintenance team to implement corrective actions.
• Trained new employee on GMP practices to equip them with the prerequisite knowledge required for all operators
• Performed label verification to ensure label information meets specification as on product master sheet.
• Trained employees on new/ updated SOPs and preformed monitoring activities to ensure compliance .
• Conducted Pre-operational inspection to ensure clean equipment and production area prior to production.
• Performed environmental monitoring swabbing/sampling, to ensure the plant meets all regulatory environmental parameters.
• performed premise audit on facility to ensure all areas meets the pre-determined requirements.
• Developed monthly, end-of-quarter and other statistical reports for leadership team and quality improvement programs.
• Inspected raw materials and finished products to verify quality and disposed items that did not meet safety requirements.
• Performed daily verifications for equipment used.
• Performed document verification for completed production worksheet to ensure accurate information
• Recorded and organized test data for report generation and analysis.
• Performed allergen monitoring to prevent contamination and cross-contamination of raw ingredients and finished products.
• Performed annual allergen validation activities
• Initiated and generated supplier report for any supplier related quality issues.
• Performed quarterly onsite and skill assessment on operators to ensure they have adequate knowledge to perform task.
• Conducted real time product quality monitoring to ensure products meet specific product parameters
• Reviewed and updated company SOPs/SSOPs to reflect current practice.
• Generated Non-compliance report for deviations/ incidents clearly identifying root course, raising corrective/preventive actions and ensuring timely implementing of corrective actions.
• Reviewed supplier certificate of analysis to ensure incoming supplies meets specification.
• Perform sensory analysis for finished products to ensure they meet organoleptic parameters.
• Ensured CTQ (critical to quality) record is updated and maintained for all products, that describes clear products characteristics critical to the customer.
• Ensured all CFIA regulatory requirement are met ,all documentations are up to date and provided when needed.

• Assured products met pre-determined specifications through careful label verification and routine operational visual inspection, weight and package integrity checks
• Evaluated samples against standards by completing measurements, visual inspections and other established tests.
• Performed thorough inspections and sampling of incoming materials
• Ensure timely and accurate documentations in accordance with good Documentation practice.
• Assured that products throughout production process are carried out in accordance with plant’s HACCP, SOP and GMP requirements.
• Collect samples during production for sensory and testing to determine product quality.
• Assured the effectiveness of cleaning procedures through pre-operational visual inspection, ATP Swabbing and operational visual inspection

• Adjudication and billing of client’s drug plan
  
• Received incoming supplies and stocked in correct locations.
• Communicated instructions to patients or caregivers about proper use and storage of drugs
• Counted and labeled prescriptions with correct item and quantity
• Answered telephones and provided information about order status, store hours and pharmacy procedures

• Advised patients on potential drug interactions and side effects, proper dose timing and medication storage.
  
• Conduct monthly inventory count and compiling end of month stock report.
  
• Placed timely and accurate supply orders to maintain optimal levels of medications, containers, labels and other consumables.
  
• Monitored medication inventory levels and kept detailed documentation in company software
  
• Maintained compliance with healthcare, industry and facility rules and regulations.
  
• Ensured accurate and up to date documentation and storage of all tool,templates and records
  
• Effective temperature maintenance and monitoring of all temperature-controlled storage areas.
  
• Ensure proper storage, packing and transportation of all cold chain items.
  
• Conduct annual supplier's audit and facility inspection to ensure their processes meets organizational standards.
  
• Received and verified daily incoming drug inventories, reported discrepancies and logged items into inventory system.
  

• Prepared and delivered product presentations and answered questions about cardiovascular product portfolio to increase sales.
• Facilitated upselling by cultivating productive relationships with clients, doctors' office staff, and clinical center personnel.
• Build and sustain extensive business relationships in key accounts across the territory.
  
• Time, resource, and territory management.
  
• Increased brand awareness by executing marketing programs ;like product detailing, clinical presentations.
  
• Increased product and brand awareness by sustaining a strong marketing presence in hospitals ,pharmacies and primary health care providers within my territory.
  

On-going online

Pharmacy Examining board of canada Evaluated as Canadian Equivalent April, 2018