Consultancy Opportunity: Â Qualitative data collector for a rapid Training Needs Assessment (TNA) for the Rwanda Food and Drugs Authority
Country:Â Rwanda
Location:Â Rwanda
IH Activity Manager: Sr. Advisor – Regulatory Workforce and Organizational Capacity Development
 IntraHealth International Rwanda Office will facilitate the hiring process and contract management.Â
When: August – October 2021 (2 months
LOE:Â 18 days
Scope of Work
I. Background:
About USP and the PQM+ Program
The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries. USP’s focus on global public health extends to lower and middle-income countries with work in over 20 countries through donor-funded programs. Our programs are focused on building the capacity of regulatory authorities and manufacturers in ensuring patient access to quality-assured essential medicines by providing: 1) technical assistance to manufacturers to increase the supply of quality-assured priority medicines for malaria, HIV/AIDS, tuberculosis (TB), neglected tropical diseases (NTDs), and maternal, newborn, and child health (MNCH) products; and 2) capacity-building activities to regulatory authorities to fulfill their function in ensuring the supply of quality-assured medical products.
USP was awarded the Promoting the Quality of Medicines Plus (PQM+) program, a USAID-funded global program designed to sustainably strengthen medical product quality assurance systems in low-and-middle income countries, including Rwanda. PQM+ is currently seeking a consultant to undertake a rapid training needs assessment for the Rwanda Food and Drugs Authority (Rwanda FDA).
Brief Description of Purpose and Nature of the Assignment
The PQM+ program is contributing to the development of the Rwanda FDA organizational capacity by targeted STTA to conduct a training needs assessment and development of a Training Plan. Rwanda FDA staff have undergone several trainings to hone their technical skills in food and medical products regulation. Rwanda FDA staff have also been trained by other partners such as the World Health Organization (WHO) and other USAID programs on various pharmaceutical regulatory functions. This TNA seeks to establish the coherence of the training solutions as they relate to demonstrable needs as relevant to the organizational structure, associated job descriptions (JDs) and in alignment with the newly released WHO regulatory competency framework. Lastly, this assignment will put in place elements that will ensure the sustainability of Rwanda FDA learning and development systems
An indicator of organizational development and the institutionalization of best practices is a system for tracking trainings that have been offered to and consumed by its staff. This and related elements such as an SOP related to how a training plan is developed, implemented and assessed for effectiveness are elements needed to align with the WHO Global Benchmarking Tool for regulatory authorities. The team will assess the Rwanda FDA’s system for tracking training and related SOPS. Ultimately, the tracking system will be a record of trainings staff have undertaken and will incorporate a structured plan of the trainings that the staff need to take to sharpen their competencies to improve work performance. In addition, as the medical products regulatory field keeps on changing, Rwanda FDA staff must continuously improve their understanding of new developments in the field. Staff learning and professional development can be achieved in many ways and the above-mentioned tracking system would help Rwanda FDA monitor learning and development throughout the organization while providing evidence for continued planning.
To achieve the above, PQM+ is seeking the services of a local workforce capacity development expert to co-facilitate the data collection and report writing required of this rapid training needs assessment to inform the development of a competency-based training plan that aligns with the WHO Regulatory competency framework and associated Global Benchmarking Tool. The workforce development consultant should have extensive experience with conducting complex assessments, collecting qualitative data collection, creating training plans, and working with government stakeholders as well as, have a familiarity with the mandate, functions and operations of a national medicines regulatory authorities, like Rwanda FDA, and the WHO regulatory competency framework.
The consultant will be working jointly with a remote technical advisor and report writer to design the methodology, develop the tools, analyze data and produce the deliverables. Both consultants are responsible for the successful engagement with stakeholders, updating the PQM+ team and delivery of tools.
The consultant will be supervised by Sr. Advisor, Workforce Development, Lauren Montgomery-Rinehart.
All work will align to PQM+ and USAID Branding (Branding TEMPLATES).
II. Key Responsibilities/Tasks
The consultant will:
Project Management Responsibilities
a)Â Participate in the initial kick-off meeting and other work implementation meetings with the PQM+ and Rwanda FDA teams to discuss the activity, agree on activity implementation plan to guide the activity through completion
b)Â Provide continuous updates to the PQM+ and Rwanda FDA teams on progress of assignment
c)Â Compile and submit notes and action points from key meetings
Supporting Documentation and websites (not exhaustive list)
III.Overall Deliverables and Timeline
What |
When |
Percentage |
Inception Report |
Week 1 |
10% |
Training Needs Assessment |
Week 4 |
20% |
Inventory/database of trainings undertaken by Rwanda FDA staff |
Week 5 |
|
Training Plan |
Week 7 |
70% |
SOP on Training Plan development |
Week 8 |
|
Guidelines on training tracker |
Week 8 |
|
Final report |
Week 9 |
Time frame for the work
The work has a level of effort of 18 workdays and will be conducted within a timeframe of approximately two (2) months between August 2021 and October 2021 (detailed timeline to be established with the consultant, in consultation with the Rwanda FDA).
IV. Payment schedule
All invoices will be approved by Lauren Montgomery-Rinehart. Payment will be made upon receipt and approval of the Consultant’s invoice. Invoices will follow the IntraHealth format as presented to Consultant in the Agreement.
V. Basic Qualifications and Experience
Other Competencies
Application Procedure
If you are interested in this consulting work, please provide us with the following:
Closing Date: The closing date for applications is August 31, 2021. However, due to the urgency of this position, applications will be short-listed and interviewed on rolling basis, and we may offer the consultancy to before the closing date. Applications should be submitted to Lauren.montgomery@usp.org with a copy to hr-rwanda@intrahealth.org with Qualitative data collector for a rapid Training Needs Assessment (TNA) for the Rwanda Food and Drugs Authority in the subject line.
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