• Bachelor’s/Master’s in Computer Science, IT, or related field. 
• 5+ years of digital project management experience specifically within a pharmaceutical manufacturing, biotech, or CDMO environment with deep knowledge of GMP/GxP.
• 3+ years of hands-on experience in large-scale ERP system implementations (e.g., SAP, Oracle), with a strong grasp of manufacturing and supply chain modules.
• Deep understanding of pharmaceutical regulatory frameworks, including Current Good Manufacturing Practices (cGMP), 21 CFR Part 11
• Proven organizational skills in managing cross-functional teams and vendors. 
• Strong project management capability; PMP/Prince2 certification preferred. 
• Native or professional fluency in English is required; Mandarin is a plus, to effectively coordinate with global teams and stakeholders. 
• Experience in multinational pharma or CDMO manufacturing sites preferred. 
• Knowledge of drug discovery and pharmaceutical process development processes preferred. 

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.