Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly experienced on SYSPRO business requires. Ensure release of 3" party products on time. Sends relevant QA reports to contract contract givers for approval. Assist with product release when required. Documentation Ensure that all queries Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical
Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical Systems, Documentation Control, Human Recourse, Production, S5 & S6 Controls Highly experienced on SYSPRO business requires. Ensure release of 3" party products on time. Sends relevant QA reports to contract contract givers for approval. Assist with product release when required. Documentation Ensure that all queries Registration with SAPC (ESSENTIAL) Minimum of 3 - 5 years' post qualification working experience in a pharmaceutical
compliance requirements and best practice. Conduct post incident investigations in order to identify root knowledge of Vector strategies, policies, customer products and operations Auditing Relationship building
compliance requirements and best practice. Conduct post incident investigations in order to identify root knowledge of Vector strategies, policies, customer products and operations Auditing Relationship building
Management to ensure appropriate oversight for products within its responsibilities. Ensure the pro-active pro-active Benefit Risk Management throughout product life cycle translating global safety data to insights Responsibility & Benefit Risk Management: Establish Product knowledge with a focus on safety profiles, Therapeutic Operating Company employees, and Adverse Event and Product Quality Complaints (AE/PQC) training to distributors/3rd-Party new/revised safety regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities)
Management to ensure appropriate oversight for products within its responsibilities. Ensure the pro-active pro-active Benefit Risk Management throughout product life cycle translating global safety data to insights Responsibility & Benefit Risk Management: Establish Product knowledge with a focus on safety profiles, Therapeutic Operating Company employees, and Adverse Event and Product Quality Complaints (AE/PQC) training to distributors/3rd-Party new/revised safety regulations (for drugs non-medicinal products & Medical Devices in the scope of responsibilities)