Over de functieWe are looking for a dynamic, hands-on individual who shares our passion for conservation and will accept the challenge of supervising the QA team.You have to be VERY HANDS ON and take responsibility for the following duties:• oversee quality operations and supervise the QA team• establish and roll-out a new QMS• compile and manage SOPs and master documents• document and review all QMS activities e.g. deviations, change controls, CAPAs etc.• create and execute a GMP training programme for all employees• approval and management of suppliers• coordinate and execute internal and external audits• oversee the validation/qualification programme• production/batch document review• compile quality reports and conduct quality reviews for presentation to managementWat wij vragenQualifications required: BSc with microbiology OR BPharm degree with active registration as a pharmacist with the SAPCExperience & skills required:• At least one years’ managerial experience• At least 3 years of QA experience in a pharmaceutical environment• Excellent knowledge of cGMP (with a focus on steriles)Soft skills:• Ability to take initiative and work independently• Excellent time management• Good analytical and problem solving skills• Exceptional attention to detailMUST BE WILLING TO RELOCATE to Nelspruit/White River, South AfricaWat wij biedenWe offer you a challenging position with plenty of room for self development and professional growth.Over het bedrijfWildlife Pharmaceuticals is a proudly South African pharmaceutical company with over 20 years of experience in small batch API and FPP manufacturing. We specialise in medicines for management of wildlife.#J-18808-Ljbffr