Project Management Director/ Senior Director

Key Responsibilities

• Develop comprehensive project plans, including scope, timelines, deliverables, and resource allocation aligned with client and operational needs
• Oversee project execution, monitor progress, and proactively address risks or issues to ensure timely and successful delivery
• Coordinate cross-functional teams across R&D, manufacturing, quality, and supply chain to ensure seamless project implementation
• Maintain strong communication with clients and external partners, providing regular updates and managing change requests effectively
• Establish and enhance project management frameworks, standard processes, and governance to improve efficiency and consistency
• Lead and develop the project management team, including performance management, training, and capability building
• Ensure compliance with regulatory standards and quality expectations throughout the project lifecycle
• Support leadership with additional strategic or operational initiatives as required

Requirements

• Master's degree or above in Life Sciences (e.g., Biochemistry, Molecular Biology, Immunology, Pharmacy) or related discipline; exceptional candidates with a Bachelor's may be considered
• At least 5 years of project management experience in biopharmaceutical CDMO or related industry
• Strong understanding of the full drug development lifecycle, from early research through commercial manufacturing
• Proven leadership experience managing cross-functional teams and delivering complex projects successfully
• Familiarity with global regulatory standards (e.g., GMP, ICH, FDA, EMA) and exposure to regulatory submissions or audits
• Proficiency in project management tools and methodologies, with strong capabilities in risk, cost, timeline, and quality management
• Excellent bilingual communication skills in English and Mandarin, with the ability to work in a dynamic, international environment