Education and Experience:

• Master's (MS) or PhD in life sciences; chemistry preferred
• A minimum of 5 years of pharmaceutical or CRO/CMO industry experience, preferably in API process R&D and manufacturing and/or Drug Product R&D and manufacturing.
• Prior experience in project management or managing external research collaborations, with PMP certification desired.
• Candidate should possess strong and effective project management, problem-solving, and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business, and operational areas.
• Demonstrates a good understanding of the pharmaceutical industry and small molecule drug development.
• Minimum of 5 years of relevant pharmaceutical or biotech industry experience in CMC process development and/or GMP manufacturing.
• Working knowledge and understanding of current regulations and industry trends for small molecule, manufacturing, and testing. Oligonucleotide and Solid State Peptide experience a plus.
• Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required.
• Must have working knowledge of MS Office products, especially MS Project.

 Independence/Accountability:

• Must be a self-starter, self-motivated, and highly flexible in this home based position with ~25% travel
• Must be organized and detail-oriented
• Problem Solving
• Proven experience in creating and carrying out successful plans and processes to solve complex problems

Leadership Activities:

• Work closely with team members across all CMC-related business units and with the STA management team to ensure coordination of all efforts and real-time communication with all stakeholders.

Communication Skills:

• Proficiency in both English and Mandarin is required.
• Excellent communication skills (verbal, written, and presentation skills).