Research and Development Director
AI summary
Microhaem Scientifics is hiring a Research and Development Director in Kampala, Uganda to lead end-to-end medical device product development, cross-functional collaboration, and R&D team leadership. The role requires a Master's degree in a relevant engineering field, 10+ years of medical device R&D experience, and strong knowledge of ISO 13485, WHO standards, and stringent regulatory requirements.
- Senior leadership role leading medical device product development from concept to commercialization
- Requires Master's degree in Biomedical, Electrical, or Systems Engineering; PhD preferred
- 10+ years of medical device R&D experience with point-of-care and rapid diagnostic tests
- Strong knowledge of ISO 13485, ISO 14971, IEC 60601, and WHO standards required
- Based in Kampala, Uganda with cross-functional collaboration across Quality, Regulatory, and Manufacturing
AI job guide
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AI salary guide
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Can you qualify for this role?
- Required10+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in sales, internship, technologyThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Research and Development Director evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Microhaem Scientifics and the role in Not specified.
- Add concrete examples related to sales, internship, technology, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Fuzu Uganda; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- Fuzu Uganda
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
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Interview preparation
- What experience makes you a strong fit for this Research and Development Director role in sales, internship?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Microhaem Scientifics before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
- Kampala
- •
- Uganda
- Contract Type
- Description
- DUTIES AND
Responsibilities
- Essential functions of the position include but are not limited to the following. Other duties may be assigned.
- A. Product Development & Technical Leadership
- Lead end-to-end product development initiatives from concept through commercialization in accordance with WHO standards, ISO 13485, ISO 14971, and IEC
- Translate user needs into product
Requirements
- and executable development plans with defined milestones, timelines, and risk mitigation strategies
- Implement sustainable research and design and product improvement activities for existing commercial-stage products.
- Drive system-level design architecture, integration strategy, and research and design decision-making.
- Ensure systematic and compliant execution of SRA-compliant design controls and
- Support development and execution of verification & validation
- Lead technical troubleshooting, root cause investigations, and field issue
- Support manufacturing supplier management and design transfer
- Support regulatory submissions and health authority interactions
- B. Cross-Functional Collaboration
- Support technical documentation development for regulatory submissions and regulatory
- Collaborate closely with Regulatory Affairs and Quality on design and development file (DDF) development, risk management, Verification & Validation, and change control
- Lead research and design activities associated with IEC 60601, IEC 62304, ISO 14971, and Human Factors Research and
- Provide support to marketing and sales team, support the introduction of new technologies with the development of presentations, sales tools, formulations, and applications data
- Communicate results to the scientific community via published papers. Present research at academic/industry symposia as an external representative of the
- C. Leadership & Team Development
- Lead and mentor team
- Help establish a high-performance research and design culture centered around accountability, technical rigor, and execution
- Coordinate internal research and design resources and external development
- Support recruiting and development of future research and design
- Collaborate cross-functionally across R&D, Quality, Manufacturing, Clinical, and Operations.
- QUALIFICATIONS &
- Master’s degree in Biomedical Research and design, Electrical Research and design, Systems Research and design, or related field PhD is preferred.
- 10+ years of
Experience
- A.
- in medical device research and
- Strong
- with point of care tests including rapid diagnostic ests,
- Startup medical device company
- strongly
- Understanding of ISO 13485 and stringent medical device regulations including
- B.
- with eQMS and requirements/risk management
- Familiarity with, statistical tools, and modern research and design collaboration platform
- Tags
- Research, academy
- Manufacturing
- Senior-level
- Uganda
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Preferred Qualifications
skills
Strong leadership skills and ability to collaborate effectively with team members and Familiarity with medical device research and design concepts, test methods, equipment and applicable national and international standards relating to testing ISO 13485, WHO and other stringent regulatory authorities (SRAs).
Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in scientific form and deal with several abstract and concrete
Ability to comprehend and communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by
Strong systems-level technical
Excellent communication and leadership
Hands-on research and design
Strong organizational and prioritization
Comfortable operating in rapidly evolving
Ability to independently drive technical
High-accountability builder
Hands-on, driven work ethic and entrepreneurial
C. Computer Software / Programs
Proficiency with Microsoft Office and technical presentation