Seeking a highly motivated scientist to join the Molecular Diagnostics team, focusedon developing regulated diagnostic products and services, especially in genetic testing, andbased onmolecular approaches such as but not limited to next-generation sequencing (NGS)-based and nucleic acid amplification-based diagnostic assays.
The successful candidate will lead the development of innovative workflows for clinical applications and work closely with clinical and commercial stakeholders to deliver successful and impactful solutions.
Key Responsibilities
- Responsible for good record-keeping and standard operating procedures (SOPs) implementation in accordance with confidential information requirement, quality system and regulatory guidelines.
- Responsible for mentoring junior scientists and coaching forthe latest technology development and product landscape.
- Responsible for prompt support and communicationwith internal and external collaborators.
- Responsible for assay planning andexecution.
- Responsible for presenting progress, findings, and providing solutions to internal and external stakeholders.
- Responsible for troubleshooting and keeping technical development timeline.
- Contribute to project scoping and preparing project proposals with in-depth understanding in clinical workflow, clinical unmet needs, technology value proposition, economic value capture, clinical deployment, and product commercialization pathway.
- Contribute to product landscape study on safety dossier and technical note approved by regulators.
- Contribute to clinical study design and clinical trial in regulated diagnostic product settings.
- Manage and perform lab operations activities, including general laboratory and equipment housekeeping and qualifications, and consumables purchasing.
Requirements
- Education in Molecular Biology, Biochemistry, Genomics, Biotechnology, or a related field.
- 3-5 years of hands‑on experience in molecular assay development, preferably in industrial, diagnostics or clinical laboratory setting.
- Laboratory track record and skills in pre-analytical and analytical techniques, including extensive knowledge and hands‑on experience in molecular techniques.
- Strong track record in experimental design and optimisation of laboratory workflows.
- Familiarity with regulatory and quality standards for diagnostic assay development e.g. ISO13485.
- Ability to multi-task, while maintaining prompt response.
- Ability to articulate complex matters and simplify the matters.
- Great presentation skills for a mixed audience.
- Strong in identifyingcritical pathways and demonstrate problem‑solving abilities.
- Solid academic knowledge and a critical and innovative mindset.
- Extensiveindustrial relation and understanding of product landscapes.
- Optimistic and enthusiastic aboutcontinuous learning and professional development in the rapidly evolving field.
- A strong team player with a proactive and upbeat attitude.