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Provision of a reliable and efficient regulatory affairs service that puts current regulatory and compliance knowledge of the plasma fractionation industry and plasma derived medicinal products to work in attaining the business goals of NBI in the manufacture and sale of safe, quality, efficacious products in accordance with registration commitments, operational requirements and internationally accepted regulatory standards and those accepted by the SAHPRA. Bachelor's Degree in Pharmacy Medicines registration and CTD/e-CTD training 3 years in the SA pharmaceutical industry in a manufacturing/quality assurance/regulatory environment. Understanding of a pharmaceutical quality system, cGMP, GPP principles and pharmaceutical legal requirements. MS Office proficiency (Word, Excel, PowerPoint, Outlook) Specific Operational Requirements • The successful candidate will be required to work an 8-hour shift. • May be required to work overtime to meet the business needs. • Must be prepared to work shifts/weekends/public holidays when needed. R65 000 CTC Apply Now

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Jobs in Go!