Pharmaceutical
QA/QC Expert,
USAID/Indonesia’s
Promoting the Quality of Medicines Midterm Evaluation, Scope of Work
 
 
Company Profile 
MSI, a Tetra Tech Company, is a Washington, DC metro area
international development firm with a 35-year history of delivering development
results across the world. Our core expertise is in the fields of monitoring and
evaluation (M&E), institutional development, public sector management,
governance and anti-corruption. For more information on MSI, please visit our
website at www.msiworldwide.com.
 
 
Project Summary
The USAID/Indonesia Monitoring & Evaluation Support Project (MESP) works to improve
the functioning and utility of USAID Mission performance monitoring, evaluation,
learning, and project design and implementation, through a combination of
direct M&E support, expert technical assistance, training, and knowledge
sharing.
 
Under MESP, MSI has been asked to conduct midterm
evaluation of Promoting the Quality of Medicines  (PQM) activities to learn the program
successes and challenges, to improve and strengthen the ongoing remaining
implementation and to identify recommendations for future investments.
 
Please note: Only Indonesian
citizens are eligible for this position
 
 
Position Summary
MSI is seeking Pharmaceutical
QA/QC Expert
to serve as Midterm Evaluation Team Members
and work under the leadership of the Team Leader and MSI for the upcoming PQM project
midterm evaluation. The purpose of this
midterm evaluation is to improve the implementation and enhance the impacts of PQM
activities. The evaluation will achieve this purpose by assessing the project’s
performance, its outcomes, its progress towards intended results, the GOI’s inter-agencies
policies and procedures for medicines quality assurance, and then recommending
ways in which implementation can be enhanced.
 
The midterm evaluation is
expected to begin in August 2017 and finish by the end of September 2017. The
anticipated level of effort for the Evaluation Specialist is approximately 55 days.
 
Responsibilities
·        
Review project
background materials
·        
Participate in the
initial Team Planning Meeting
·        
Contribute to the
development of the design of midterm evaluation, including the research methodology,
data collection instruments and sampling plan, and workplan
·        
Contribute to the
writing of midterm evaluation reports (draft and final), and debriefing
·        
Support and participate
in quantitative and qualitative data collection, which may include desk review,
key informant interviews, and/or focus group discussions in Jakarta and
multiple provinces
·        
Contribute to
coordinating a Findings/Conclusions/Recommendations Workshop in Jakarta as well
as a final workshop with Government of Indonesia officials
·        
Other tasks, as
assigned by the Team Leader or MSI
 
Required Qualifications

• Master’s degree or higher in relevant field
  required
• At least 7 years’ of professional
  experience working on the field of pharmaceutical supply and system, health
  system and policy in Indonesia
• Experience evaluating projects in health
  sector, preferably in pharmaceutical topic
• Required strong knowledge on Indonesia’s
  medicines quality assurance / quality control system, and health system
  and policy
• Has professional networking with BPOM and
  Ministry of Health
• Basic research skills including experience
  conducting structure/semi-structure interviews, focus group discussion and
  designing/administering survey
• Experience working on evaluation team
  under donor-funded projects preferred
• Excellent writing and inter-personal
  communications skills
• Fluency in English language preferred

 
 
Deliverables
·        
Midterm
evaluation designs and work plans, including detailed methodology, data
collection instruments, sampling plan and implementation plan schedule
·        
Final
midterm evaluation report
 
 
Only
candidates who have been selected for an interview will be contacted. No phone
calls, please.
MSI is an EEO/AA/ADA Veterans
Employer.
 

To apply: Please submit your CV with subject ‘PQM : PHARMACEUTICAL
QA/QC EXPERT’ and email to: [email protected]

No later than July 19, 2017