Requirements

Applicants must be in possession of a Matric certificate and an appropriate degree in Nuclear Medicine/Radiography/ Biomedical Engineering/Diagnostic Radiographer/Physics/Medical Physics or related equivalent qualification at NQF level 8 as recognised by the South African Qualifications Authority (SAQA). Professional registration with the HPCSA (current registration to be submitted with application). Valid driver’s license. 

Experience

Minimum of three (3) years working as Clinical Engineer/Biomedical Engineer/Diagnostic Radiographer. Working knowledge of and experience in relevant national legislation and international standards. Computer Literate. Working experience in administration, data management and supervisory skills will be an added advantage. 

Competencies, Technical Proficiencies, and Values 

*Comprehensive knowledge and understanding of relevant legislation, protocols, standard operating procedures, and work instructions. *Self-motivated and able to work independently. *Ability to manage a variety of crossfunctional team members. *Competent in problem-solving, research skills and team building. *Attention to detail, Information evaluation decision-making, objectivity, resilience, communication skills (verbal, written, negotiation, conflict management, presentation). *Interpersonal skills. *Assertiveness, ethical behaviour, customer service, planning and organising skills. *Team management. *MS Office. *Ethical behaviour and adherence to the SAHPRA Code of Conduct. At SAHPRA we adhere to our core values: Ubuntu, Responsiveness, Integrity, Transparency, Efficiency, Excellence. 

Duties

Review and verify license applications for completeness, correctness, and compliance. Utilise database to process licence applications for listed electronic products. Reconcile receipts and follow up on incomplete transactions. Follow up on defaulters and dispatch renewal notifications. Follow up on defaulters of annual returns through inspections. Support the Deputy Manager and Senior Manager to respond to the queries from the industry related to the listed electronic products. Engage with industry stakeholders through training/workshop to enhance compliance with regulatory requirements of listed electronic products for non-ionising devices. Processing import and export authorities. Process radiation over-exposure notifications. Compile and update a register for all radioactive sources.