A biotech start-up with a strong product focus on therapeutic vaccines Reports to Head of Technology & Operations Role focused on CMC / pharmaceutical manufacturing control Summary We are partnering with a biotech start-up pharmaceutical group to
A prominent pharmaceutical group with a broad and diversified product portfolio Reports to Head of Regulatory Affairs Role focused on submission and communication with regulators Summary We are partnering with a prestigious pharmaceutical group to recruit
Bitget is one of the worlds leading digital assets ecosystems. With over 120 million registered users, Bitget has one of the most comprehensive suites of blockchain products and services available via bitget.com. Our mission is to
A prominent pharmaceutical group with a broad and diversified product portfolio Reports to Head of Regulatory Affairs Role focused on submission and communication with regulators Summary We are partnering with a prestigious pharmaceutical group to recruit
Responsibilities 1- Regulatory Strategy Development Lead New Drug Application (NDA) submissions and approvals for oncology and innovative products in Hong Kong and Macao. Track latest regulations from the Hong Kong DOH Pharmacy and Poisons Board (PnPB) and
Key Accountabilities Responsible to establish and maintain a group of high performing regulatory affairs professionals working in an efficient, productive and harmonized fashion to support the execution of company plans in Hong Kong. Closely collaborate with
Position Purpose This position serves to provide operational support in Hong Kong regulatory management. This includes, but not limited to, defining and executing aligned regulatory strategies for new and existing products, including all developmental and lifecycle
Key Responsibilities: Develop and implement procurement strategies aligned with company priorities and budget constraints. Establish procurement policies, processes, templates (RFPs, contracts, vendor evaluation frameworks) across preclinical, clinical and CMC activities. Lead sourcing, evaluation, and selection of CROs,
Primary Responsibilities Non-clinical development strategy and execution For in vivo gene editing pipelines (e.g., liver targeting, ophthalmology, central nervous system, etc.), independently develop and lead high-quality non-clinical pharmacology, pharmacokinetics, and toxicology study strategies in full compliance with