of estimating time required to manufacture the product.
Amendments to include price adjustments, additional product or service items, technical service items, etc clarifications, payment schedules Implement and control product and supplier consolidations Perform ‘Total Cost and control of Applications for all master data (product catalogue and suppliers) Assist with commodity and inventory management Familiarity of plant product catalogue Computer literate in MS Office The post
AND PRODUCTION
Skills Requirements
Amendments to include price adjustments, additional product or service items, technical service items, etc clarifications, payment schedules Implement and control product and supplier consolidations Perform ‘Total Cost and control of Applications for all master data (product catalogue and suppliers) Assist with commodity and inventory management Familiarity of plant product catalogue Computer literate in MS Office The post
technical qualification
account
concerning both registered and to be registered products. Ensuring cGMP and statutory compliance (wrt the pharmacovigilance issues as per relevant guidelines for the product portfolio. DUTIES AND RESPONSIBILITIES Perform all regulatory affairs issues pertaining to our products and our facilities. 14. Renewal of drug registrations registrations locally and in other countries where products are registered. 15. Conducting Internal Quality actively monitor the safety of authorized medicinal products and detect any change to their risk-benefit balance
Description GRADUATE Purpose of the job is to assist the Product Management team with daily functions including Development: Personal development in line with Jasco Product Management functional tasks. Ensure that all administration with the research of New Products / Solutions which form part of the product management domain Business Business template/s assistance: Assist the Product Management team with the periodic updates and changes to processes Market exposure activities: Assist the Product Management team with the planning and execution
concerning both registered and to be registered products. Ensuring cGMP and statutory compliance (wrt the pharmacovigilance issues as per relevant guidelines for the product portfolio. DUTIES AND RESPONSIBILITIES Perform all regulatory affairs issues pertaining to our products and our facilities. 14. Renewal of drug registrations registrations locally and in other countries where products are registered. 15. Conducting Internal Quality actively monitor the safety of authorized medicinal products and detect any change to their risk-benefit balance
Assurance for the manufacturing of sterile injectable products Previous experience in Quality Assurance and/or quality testing of active substances and medicinal products would be advantageous Consultant: Tamsyn Best