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PATH current employees - please log in and apply Here PATH is a global nonprofit dedicated to achieving health equity. With more than 40 years of experience forging multisector partnerships and with expertise in science,…
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The Senior Program Officer will provide technical leadership to strengthen Indonesia's diagnostics and medical devices ecosystem by developing national strategic frameworks. They will engage with government agencies, manufacturers, and regulatory bodies to facilitate innovation, quality standards, and equitable access to health technologies.
Candidates must hold a postgraduate degree in a relevant field such as Biomedical Engineering, Public Health, or Microbiology. A minimum of 5–6 years of professional experience in diagnostics, medical devices, or laboratory systems is required, along with proven ability to work with government and industry stakeholders.
PATH current employees - please log in and apply Here
PATH is a global nonprofit dedicated to achieving health equity. With more than 40 years of experience forging multisector partnerships and with expertise in science, economics, technology, advocacy, and dozens of other specialties, PATH develops and scales up innovative solutions to the world’s most pressing health challenges.
Project Background
Indonesia's Health Security 2045 vision prioritizes strengthening national self-reliance in medical devices, diagnostics, and in-vitro diagnostics (IVDs), while expanding domestic manufacturing capacity. The vision further emphasizes regulatory excellence, innovation, and equitable access to quality diagnostics across disease areas.
PATH is supporting the Ministry of Health (MoH), Indonesia, and key national stakeholders to develop a strategic roadmap for medical devices and diagnostics, identify innovative technologies, strengthen regulatory pathways, and build an enabling ecosystem for sustainable diagnostics scale-up.
Position Summary
PATH is seeking an experienced Senior Program Officer/ Program Officer-Diagnostics to provide technical leadership and strategic guidance in strengthening Indonesia's diagnostics and medical devices ecosystem. The consultant will support the development of a national strategic framework and implementation roadmap, assess innovative diagnostics technologies, engage with manufacturers and regulatory stakeholders, and contribute to policies and recommendations that advance diagnostics access and national self-reliance.
The role requires close collaboration with government agencies, regulatory bodies, laboratory networks, industry partners, and development organizations to support Indonesia's Health Security 2045 objectives.
Location - Delhi / Jakarta
Key Responsibilities
Technical Leadership and Strategy
Provide technical leadership across project workstreams related to diagnostics, in-vitro diagnostics (IVDs), and medical devices.
Support the development of a National Strategic Framework and Implementation Roadmap for medical devices and diagnostics in Indonesia.
Advise on strategies to strengthen diagnostics access, local manufacturing, and innovation ecosystems.
Contribute technical expertise on emerging diagnostic technologies and market trends relevant to Indonesia's public health priorities.
Diagnostics and Technology Assessment
Identify, assess, and curate innovative diagnostic technologies, IVDs, and medical devices with potential for adoption and scale-up.
Evaluate technologies based on public health relevance, feasibility, scalability, manufacturing potential, and regulatory readiness.
Conduct assessments of local manufacturing capabilities and opportunities for strengthening domestic production.
Support evidence generation and prioritization of technologies aligned with national health needs.
Stakeholder Engagement and Industry Collaboration
Engage with national and international diagnostics and medical device manufacturers, industry associations, and private sector partners.
Collaborate closely with the Ministry of Health, including the Directorate of Medical Devices, Department of Health Laboratories, and relevant technical units.
Facilitate stakeholder consultations, workshops, technical working groups, and expert discussions.
Maintain effective communication and coordination between PATH and government counterparts.
Regulatory and Quality Systems Support
Provide technical inputs on regulatory pathways, standards, quality management systems, and market authorization processes for diagnostics and medical devices.
Support work related to ISO 13485 compliance, validation and verification processes, laboratory quality systems, and regulatory best practices.
Contribute to health technology assessment (HTA)-related activities and evidence-based decision-making processes.
Identify opportunities to strengthen regulatory and policy frameworks supporting diagnostics innovation and scale-up.
Expected Deliverables
Documentation and technical input supporting the National Strategic Framework and Implementation Roadmap for medical devices and IVDs.
Technical assessment report on diagnostic technologies, innovation landscape, and local manufacturing capabilities in Indonesia.
Recommendations on priority diagnostics and medical devices for scale-up and ecosystem strengthening.
Technical inputs on regulatory pathways, quality systems, validation frameworks, and HTA considerations.
Reports from stakeholder consultations, workshops, technical working groups, and expert engagements.
Policy briefs, technical notes, and knowledge products for government, industry, donor, and technical audiences.
Required Qualifications
Education
Postgraduate degree in Biomedical Engineering, Biotechnology, Microbiology, Clinical Laboratory Sciences, Public Health, Health Technology, or a related field.
Experience
Minimum 5–6 years of professional experience in diagnostics, medical devices, laboratory systems, health technology innovation, or related fields.
Experience supporting the development, introduction, evaluation, or scale-up of diagnostic technologies within healthcare or public health systems.
Experience working with medical device manufacturers, diagnostics companies, laboratory networks, or regulatory agencies.
Demonstrated experience supporting donor-funded, government-led, or multi-country health programs.
Proven experience engaging with ministries of health, development partners, industry stakeholders, and technical agencies.
Preferred Experience
Familiarity with IVD product development pathways and diagnostics innovation ecosystems.
Experience working with quality management systems and standards, including ISO 13485.
Knowledge of validation and verification processes, laboratory accreditation systems, and regulatory best practices.
Experience supporting Health Technology Assessment (HTA) processes and evidence-based policy development.
Prior experience working in Indonesia or Southeast Asia.
Familiarity with Indonesian health sector institutions, including MoH, BPOM, BSN, provincial health offices, national public laboratories, and related stakeholders.
Skills and Competencies
Strong technical expertise in diagnostics, IVDs, and medical devices.
Knowledge of regulatory systems, quality standards, HTA methodologies, and laboratory strengthening approaches.
Excellent stakeholder engagement and facilitation skills. Strong analytical, report-writing, and presentation capabilities.
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