Job Description
📋 Description Lead external manufacturing strategy for small molecules and related assets. Manage CMC planning, budgets, and phase-gate governance. Guide CROs/CDMOs on process development and scale-up. Influence cross-functional decisions across asset teams and functions. Drive supply risk mitigation and supplier relationship management. Represent AbbVie in partnerships and in-licensing activities. 🎯 Requirements PhD in Process Chemistry with 8+ yrs pharma/biotech, or MS with 10+ yrs. Extensive small molecule process development, cGMP, tech transfer. Strong CMC regulatory, quality systems, and process safety knowledge. Proven ability to manage multiple projects and external partners. Influence across scientific, operational, and leadership teams. Willingness to travel up to 25% domestically/internationally. 🎁 Benefits Comprehensive benefits including medical, dental, and vision. Paid time off for vacation, holidays, and sick leave. 401(k) retirement plan with company matching. Eligibility for long-term incentive programs.
