The South African Health Products Regulatory Authority (SAHPRA), is the National Medicines Regulatory Authority established in terms of the Medicines and Related Substances Act, 1965, (Act No. 101 of 1965) as amended, to provide for the monitoring, evaluation, regulation, investigation, inspection, registration and control of medicines, scheduled substances,...
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Plan and perform inspections in accordance with the Hazardous Substances Act, related regulations and code of practice, Prepare formal reports of your finding/s during inspections,
Participate in inspection activities involving high-risk electronic generators of ionising radiation, such as linear accelerators, cyclotrons, industrial radiography etc,
Verification of quality control tests from licence holders’ equipment as prescribed by national standards, Receive and investigate incidents and accidents as reported by licence holders,
Receive and investigate occupational radiation overexposures from licence holders as supplied by approved dosimetry laboratories,
Developing and implementing of guidelines, code of conducts and standard operating procedures, Receive and respond to various queries received by the subunit in accordance with query management standard procedure.
Qualification :
Matric certificate plus a BSc Hons Medical Physics
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