Deskripsi Pekerjaan
Join A*STAR, Singapore's premier public research agency, as a Project Manager in our Digital Diagnostics division. Lead transformative medical device software projects from conception to commercialization, driving innovation in healthcare technology. You'll orchestrate cross-functional teams of engineers, clinicians, and regulatory experts to deliver cutting-edge diagnostic solutions that impact patient lives globally. This role offers the unique opportunity to shape the future of digital health while working in Singapore's dynamic scientific ecosystem. A*STAR provides comprehensive professional development resources and a collaborative environment where your project management expertise will thrive.
As a key player in our digital health initiatives, you'll navigate complex product lifecycles while ensuring compliance with stringent medical device regulations. Your leadership will be instrumental in bridging technical innovation with clinical needs, creating scalable solutions that meet global healthcare challenges. If you're passionate about leveraging technology to improve diagnostics and possess a proven track record in managing complex software projects, this is your chance to contribute to life-changing innovations at the forefront of scientific research.
Tanggung Jawab
- End-to-end lifecycle management of medical device software projects from concept to regulatory approval and commercial launch
- Develop and execute project roadmaps with clear milestones, deliverables, and resource allocation plans
- Coordinate cross-functional teams including software engineers, UX designers, clinical specialists, and regulatory affairs professionals
- Implement Agile/Scrum methodologies while ensuring compliance with medical device standards (IEC 62304, FDA 21 CFR Part 820)
- Manage project budgets, timelines, and risks using industry-standard tools and methodologies
- Facilitate stakeholder communication and presentations to executive leadership and external partners
- Drive quality assurance processes including risk management, validation protocols, and documentation
- Monitor market trends and regulatory changes to inform project adaptations and ensure competitive positioning
Kualifikasi
- Bachelor's degree in Engineering, Computer Science, Life Sciences, or related field; Master's or PhD preferred
- Minimum 5 years of project management experience in medical device or healthcare technology development
- Proven expertise in managing software development lifecycles for regulated healthcare products
- Strong knowledge of Agile/Scrum methodologies and project management tools (Jira, MS Project, Asana)
- Familiarity with medical device regulatory requirements (FDA, EU MDR, Singapore HSA)
- Certification in PMP, PRINCE2, or equivalent project management methodology
- Exceptional leadership and communication skills with ability to influence diverse stakeholders
- Experience with risk management frameworks and quality system standards (ISO 13485)