Ref.
2026/ILE/15918
Job offer type
Experts
Type of contract
Service contract
Deadline date
2026/08/15 23:59
Duration of the assignment
Beaded expertise
Contract
Freelancer
Duration
1 an renouvelable
Département Santé - DEPSAN > Pôle Renforcement des systèmes de santé
Published on : 2026/07/28
SUB-SAHARAN AFRICA
KENYA
The post is home-based with field missions to 13 countries of the project. The incumbent will work under the overall supervision of the Team Leader and the Programme Management Unit of Project Medisafe Phase 2 and under the direct supervision of the Lead Legal Expert.
Responsibilities
Within assigned authority, the incumbent will be responsible for the following specific duties:
· Support knowledge transfer and training-of-trainers initiatives aimed at strengthening sustainable national training capacities.
· Conduct training needs assessments and advisory missions.
Substandard and Falsified Medical Products (SFMP) constitute a major health, economic and security threat in Africa. The World Health Organization estimates that one in ten medical products circulating in low- and middle-income countries is substandard or falsified, causing more than 250 000 preventable deaths per year. In response to this challenge, Expertise France is implementing the MEDISAFE Phase 2 programme with the financial support of the European Union (NDICI).
MEDISAFE Phase 1 (2018-2023) covered 11 countries in East and Central Africa (Burundi, DRC, Ghana, Ethiopia, Seychelles, Kenya, Uganda, Tanzania, Malawi, Rwanda and Zambia). It produced the Reference Manual on SFMP Legislation - An African Perspective, A National Pharmaceutical Supply Chain Security Guide, A Communication Strategy on SFMP, as well as the roadmap adopted in Nairobi in April 2022. It brought together more than 300 participants across 14 regional and national events, in partnership with the European Union CBRN Network, the African Union, AUDA-NEPAD, UNODC, WHO (HQ. Geneva) and WHO AFRO (Brazzaville), INTERPOL HQ in Lyon, France, INTERPOL Regional Bureau in Nairobi, INTERPOL National Central Bureaus (NCBs) and the Council of Europe.
MEDISAFE 2.0 extends and broadens this first phase: a four-year project, funded by the European Union (NDICI) for a total amount of EUR 9 000 000, implemented by Expertise France under indirect management via a contribution agreement with the European Union Delegation (EUD) in Nigeria. It covers 13 countries grouped in two regional clusters:
Cluster A (West Africa): Benin, Côte d'Ivoire, Ghana, Guinea (Conakry), Nigeria, Senegal, Togo.
Cluster B (East and Southern Africa): Burundi, Democratic Republic of the Congo, Ethiopia, Kenya, Rwanda, Zambia.
In line with the action document approach, the project distinguishes the countries that benefited from MEDISAFE Phase 1, seven of the 13 namely Ghana, Burundi, DRC, Ethiopia, Kenya, Rwanda and Zambia, from the newly added countries. It combines activities tailored to the maturity level of the new countries, capitalization, lessons learnt, consolidation of activities for the former, and cross-cutting regional activities bringing the two groups together (peer mentoring, experience-sharing, operational coordination).
Overall objective: To mitigate the health, economic and security threats posed by (SFMP) in West and East Africa.
The project pursues this objective through three complementary specific objectives, linked within a single theory of change and all embodying an inclusive and gender-sensitive approach:
• SO1 - National and regional legal capacities to combat SFMP are strengthened through an inclusive and gender-sensitive harmonization of legal frameworks and the implementation of key regulations.
• SO2 - The capacity of national and regional legal and law enforcement actors to detect, investigate and combat SFMP is strengthened through the optimization of inclusive operational procedures, improved intelligence and the development of transnational cooperation responding to the specific needs of the most vulnerable, in particular women and children.
• SO3 - The supply chain is strengthened and secured, and public awareness of SFMP is increased, through inclusive and gender-sensitive approaches, by promoting the active role of women health professionals, women-led community-based organizations and caregivers, in order to ensure people's safety and equitable access to safe and effective medical products.
Specific Objective (SO1): The national and regional legal capacities to fight SFMP are enhanced through inclusive and gender responsive harmonization of legal frameworks and implementation of key regulations
These terms of reference fall under the legal component (SO1), to which two outputs contribute:
Contributing to SO1
OP 1.1 By 2030, at least ten partner countries have aligned national pharmaceutical and penal legislation with the AU Model Law and Medicrime Convention, incorporating clear definitions, offences, and sanctions related to SFMP. Each country will have conducted at least one national legal gap assessment validated by the Ministry of Justice and Health.
OP 1.2 At least six regulatory or procedural instruments (e.g. inspection protocols, post-marketing surveillance guidelines, or traceability regulations) are operationalized and applied by NRAs.
Competencies
Education
Advanced university degree (Master’s degree or equivalent) in Law, International Law, or in a related field, is required. A first-level university degree in similar fields in combination with two additional years of qualifying experience may be accepted in lieu of the advanced university degree.
Work Experience
A minimum of seven years of progressively responsible professional experience in designing, managing and implementing large complex programmes in law is required. Work with an international or regional organization is an advantage. Work experience in programme and project management, and coordination or a related area, at the national and the international level, with a proven track record of successfully undertaking capacity-building and mentoring is required. Work experience with national or international Legal institutions or bodies, regulatory agencies in promoting inter-agency coordination and cross-border cooperation with relevant authorities is required. Work experience in developing, deploying, and delivering technological tools, intelligence-sharing systems, capacity building programmes, and training to legal or regulatory officers in developing countries is desirable.
Languages
A high proficiency in spoken, reading and writing English and/or French are required.
Assessment
Evaluation of qualified candidates may include an assessment exercise which may be followed by competency-based interview.
Indicative volume
As required (targeted mobilisation, extensible according to the country’s needs).
Assessment
Evaluation of qualified candidates may include an assessment exercise which may be followed by competency-based interview.
Indicative volume
As required (targeted mobilisation, extensible according to the country’s needs).
Contract for a period of one year, renewable
The selection process for candidates will be based on the following criteria :
Deadline for application : 2026/08/15 23:59
File(s) attached : ToR_International_Legal_Expert_RA_28.07.2026.docx
Expertise France is the public agency for designing and implementing international technical cooperation projects. The agency operates around four key priorities :
In these areas, Expertise France conducts capacity-building initiatives and manages project implementation, leveraging technical expertise and acting as a project coordinator. This involves combining public sector expertise with private sector skills to drive impactful results.