The candidate is required to:
- Line management of project managers and development scientists within the department
- Resource management and planning, e.g. budgeting, human resource allocation, etc.
- Strategic and technical evaluation for new project scouting and development.
- Communicate regularly and effectively with researchers, clinicians and industry to conceptualize and design novel, clinically relevant and commercially viable medical device products.
- Work with both internal and external stakeholders to define project plans and budgets, develop and maintain project timelines, establish and monitor project risks and risk register and lead the project teams to achieve project deliverables and objectives in accordance to ISO 13485.
- Evaluate, initiate and execute medical device product development projects of various developmental stages towards commercialization.
- Communicate regularly and effectively with researchers, clinicians
The candidate is required to:
- Line management of project managers and development scientists within the department
- Resource management and planning, e.g. budgeting, human resource allocation, etc.
- Strategic and technical evaluation for new project scouting and development.
- Communicate regularly and effectively with researchers, clinicians and industry to conceptualize and design novel, clinically relevant and commercially viable medical device products.
- Work with both internal and external stakeholders to define project plans and budgets, develop and maintain project timelines, establish and monitor project risks and risk register and lead the project teams to achieve project deliverables and objectives in accordance to ISO 13485.
- Evaluate, initiate and execute medical device product development projects of various developmental stages towards commercialization.
- Communicate regularly and effectively with researchers, clinicians
Requirements:
Technical Skills:
- Subject matter expert in molecular diagnostics with a solid comprehension of the key industry trends and competitive landscape.
- Knowledge and track records in molecular diagnostics development, pilot and scale-up manufacturing, analytical verification, and clinical validation.
- Experience in applying design control and phase gate-driven product development processes for the development of molecular diagnostics assays and systems under ISO 13485.
- Experience in managing development projects in an IVD setting, as well as multi-project experience is highly desired
- Good understanding of applicable IVD medical device regulations, FDA design control process, and ISO 13485 standards preferred
Soft Skills:
- Experience in stakeholder management and alignment in public institution settings.
- Resourceful, strong communication and adaptability in a fast-paced environment.
- Leadership experience and ability to coach and train team members
- Experienced in originating and building strategic partnerships.
Qualifications:
- Advanced education degree or equivalent in Life Sciences, Biotechnology or related field supported
- 10+ years of similar experience
The above eligibility criteria are not exhaustive. A*STAR may include additional selection criteria based on its prevailing recruitment policies. These policies may be amended from time to time without notice. We regret that only shortlisted candidates will be notified.
