REGULATORY OFFICER : INSPECTIONS & LICENSING – Botswana Medicines Regulatory Authority 731 views

DESCRIPTION
The Botswana Medicines Regulatory Authority (BoMRA) is a body that was established through the Medicines and Related Substances Act of 2013, to regulate the supply chain of Human and Veterinary medicines, Medical Devices and Cosmetics. The Authority is looking for professionals to join their growing teams.

JOB TITLE: REGULATORY OFFICER – INSPECTIONS & LICENSING (X2)
REPORTS TO: Manager, Inspection and Licensing
JOB PURPOSE:
The Regulatory Officer will carry out inspections of drug outlets dealing in the manufacture, handling import and distribution of drugs and other healthcare products for compliance with the Medicines and Related Substances Act.
MAIN DUTIES:
To inspect premises and facilities that manufacture, distribute, dispense or keep custody of pharmaceutical and other health care products for suitability.
To actively facilitate the importation and exportation of pharmaceutical and healthcare products by inspecting drug consignments and collaborating with other customs agencies and agents.
To actively contribute to the implementation and continuous improvement of registration and assessment, inspection and licensing processes. To prepare status reports on licenses, permits, imports, transit and exports of pharmaceutical products and medical devices.
To provide support to the enforcement function through the provision of information on non- compliant facilities for further investigation.
To carry out stakeholder engagements and public education to enhance transparency in regulatory processes and requirements seize and detain unwanted products in circulation on the local market.
To develop and maintain good relations with both internal and external clients
QUALIFICATIONS:
Academic Qualifications: The ideal candidate should hold a Bachelor’s degree in Pharmacy, Veterinary, Medicine, Dental surgery, and Biomedical sciences. A qualification in Law from a recognized Institution will be an added advantage. Work experience: At least three years of working experience in a reputable pharmaceutical establishment; Previous experience in regulatory affairs is an advantage