Registration Officer-Human Medicines (x10)

  • Short Term Contract
  • Lusaka, Zambia
  • Applications have closed.

Zambia Medicines Regulatory Authority

ZAMRA wishes to invite applications from suitably qualified and experienced persons who are ambitious, innovative, energetic and performance-driven to be engaged on a short-term contract for a period of ten (10) months.

About Zambia Medicines Regulatory Authority

The Zambia Medicines Regulatory Authority (ZAMRA) was set up by the Medicines and Allied Substances Act (No. 3) of 2013 as a statutory body responsible for medicine and allied substances regulation in Zambia.

ZAMRA’s vision is to be a leader and centre of excellence in regulation of medicines and allied substances. Its mission is to protect and enhance public and animal health through the regulation of medicines and allied substances.

Registration Officer-Human Medicines (x10)


To undertake registration of medicines in order to achieve compliance to set standards of quality, safety and efficacy.


  • Undertakes effectively, the registration of medicines for human use in order to authorize their use;
  • Undertakes effectively, the maintenance of the medicines information management system in order to facilitate storage, processing, retrieval and dissemination of information;
  • Undertakes effectively the screening of applications for registration of medicines for human in order to ascertain their completeness and validity; and


  • Full Form V/Grade 12 School Certificate with five (5) ‘O’Levels with credit or better, including Mathematics and English;
  • Bachelor of Pharmacy/Pharmaceutical Engineering/Pharmacology/Biochemistry/Biotechnology/Biomedical Science;
  • Must be a member of the Health Professions Council of Zambia (HPCZ) with valid practicing Certificate or any relevant Professional Body; and
  • MSc in Regulatory Affairs and Pharmaceutics will be an added advantage


  • Basic experience:
  • Demonstrated experience in medicines regulatory processes.

Desirable experience:

  • Experience in pharmaceutical manufacturing industry.
  • Experience in maintenance of database.


  • Interpersonal skills;
  • Integrity;
  • Confidentiality;
  • Must be of sober character,
  • Ability to write reports; and
  • Able to communicate in English.

Applicants who meet the above qualifications MUST:

Submit a signed application letter accompanied by a detailed Curriculum Vitae including three (3) traceable referees and day time telephone numbers and contact addresses.

All applications should reach the undersigned not later than 2nd December, 2022.

The Acting Director-General
Zambia Medicines Regulatory Authority
Plot No. 2350/M, Off Kenneth International Airport Road,
P.O. BOX 31890,

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