Our client is a premier, home-grown Pharmaceutical Manufacturer with a dominant market position in Hong Kong and a growing footprint in the Greater Bay Area. Known for their high-quality portfolio of OTC, Rx, and consumer health products.
We are seeking a visionary Head of R&D and Regulatory & Medical Affairs to report directly to the CEO. This is a newly defined, executive-level role designed to bridge scientific innovation with commercial strategy. You will oversee a combined team of a dozen professionals, steering the product lifecycle from concept to market launch.
why this role.
- Strategic Impact: You will sit on the senior leadership team, translating business goals into scientific reality.
- Scope: You are not just running a lab; you are overseeing the entire ecosystem: R&D and Regulatory Strategy.
- Expansion: Lead the technical strategy for market expansion into China and the wider region.
about the job.
- Scientific Leadership: Provide strategic direction for all R&D activities, driving formulation development and analytical data standards to meet diverse market requirements.
- Regulatory Command: Develop comprehensive regulatory strategies to achieve rapid product approvals and renewals, specifically navigating the landscape in Hong Kong and China.
- Portfolio Management: Oversee the full lifecycle of the product portfolio (OTC, Rx, and supplements), ensuring pipelines align with corporate objectives and resource allocation.
- Cross-Functional Synergy: Partner closely with GMP manufacturing (QA/QC/Production) and Business Development to ensure integrated product strategies and evaluate in-licensing opportunities.
- Team Development: Inspire and direct a multidisciplinary team, fostering a culture of innovation while mentoring senior managers and technical staff.
skills & experiences required.
- Education: M.D., Ph.D., or Pharm.D. in a life sciences discipline is required.
- Experience: Minimum of 15 years of progressive leadership experience in the Pharmaceutical or Biotech industry.
- Track Record: Proven success in leading integrated R&D/RMA teams and driving multiple compounds from discovery to regulatory approval.
- Regulatory Expertise: In-depth knowledge of global regulatory requirements (FDA, ICH, EMA) and direct experience with major health authorities. Experience with NMPA (China) is highly preferred.
- Leadership Style: A strategic thinker with the ability to influence senior management and external partners.