Manager, Business Development and Regulatory Affairs (Ref: CNRM2026-015)
# Manager, Business Development and Regulatory Affairs (Ref: CNRM2026-015) **Centre for Novostics** · Sha Tin, New Territories · `On-site` 🕒 **Статус:** *Опубликовано: вчера* · *Источник: Indeed* --- ### About the Role Center for Neuromusculoskeletal Restorative Medicine (CNRM) Limited CNRM based at the Hong Kong Science and Technology Park (HKSTP), combines the talents and expertise in stem cells, biomaterials, 3D bioprinting, tissue engineering, and personalized and translational medicine from The Chinese University of Hong Kong (CUHK). The Center is a multi-disciplinary, international consortium devoted to the application of convergent principles and technologies of biomedical science and engineering to restore structure and function to neuromusculoskeletal tissues and organs injured, diseased and degenerated due to aging, for the maintenance of mobility and enhancement of quality of life through biomedical research and development. Key Responsibilities: 1. Identify, evaluate and pursue new business development opportunities, including partnerships, collaborations and market expansion initiatives within the pharmaceuticals and medical devices space 2. Develop and implement regulatory strategies to support product launches and market entry across different regions and jurisdictions 3. Conduct market analysis and competitive landscape assessments to inform business strategy and positioning 4. Prepare and manage regulatory submissions, including dossiers and applications to relevant regulatory authorities 5. Facilitate contract negotiation and agreement management with research collaborators 6. Liaise with regulatory bodies, stakeholders and government agencies to facilitate approvals and maintain compliance 7. Lead cross-functional teams and project management initiatives to support business development and regulatory objectives 8. Monitor changes in regulatory requirements and industry standards Job requirements: 1. Master’s degree or above in Biomedical Sciences, Biotechnology, Biochemistry, Pharmacy, or related fields 2. Previous working experience in regulatory affairs, clinical trials, pharmacovigilance, and compliance is highly valued 3. Highly independent and responsible, positive attitude 4. Strong project management skills and time management 5. Attention to details, good problem-solving skills, and decision-making 6. Excellent communication and interpersonal skills 7.Detail-oriented with strong analytical and problem-solving skills; Good verbal and written communication skills in English and Chinese The appointment will initially be made on a contract basis commencing as soon as possible, renewable subject to good performance and mutual agreement. The information provided will be kept confidential and only be used for those purposes relating to your application. We are an equal opportunities employer and welcomes applications from all qualified candidates. Work Location: In person
Наблюдалась 2026-10-15, впервые 2026-10-13, источник — Indeed.