Director of CMC, External Operations

• Develop and execute CMC strategies aligned with clinical development timelines and regulatory requirements. Serve as a CMC lead on AbbVie's project team.
• Identify, evaluate, select and manage CMO/CDMO partners based on technical capabilities, quality systems, capacity, timelines, and cost considerations. Lead due diligence and technical assessment of potential manufacturing partners.
• Lead the negotiation of the Manufacturing Service Agreement, ensure that effective planning and materials procurement strategies are in place.
• Establish effective governance models with external partners, including communication plans, oversight strategies, project milestones, risk management, and performance monitoring.
• Serve as the primary AbbVie CMC point of contact and ensure successful execution of outsourced activities, including process development, analytical development, formulation development, GMP manufacturing, fill-finish, packaging, and stability studies. Monitor progress, identify potential technical and operational risks and implement mitigation strategies.
• Review and provide technical oversight of manufacturing processes, batch records, process characterization, and technology transfer activities.
• Partner with Quality Assurance, Regulatory Affairs to ensure compliance with applicable GMP and regulatory requirements. Ensure timely delivery of clinical trial materials.
• Provide CMC input into regulatory submissions, including IND/CTA, IMPD, and other global filings.
• Oversee preparation and review of CMC documentation, including Module 3 sections and supporting technical documents, supporting regulatory interactions related to CMC activities.
• Collaboration with cross-functional teams including research, nonclinical, clinical operations, regulatory affairs, and clinical drug supply teams to support program advancement. Maintain ongoing communication with the appropriate AbbVie US stakeholders about CMC progress, risks, and recommendations throughout the manufacturing cycle.

Qualifications

• PhD, MS, or equivalent degree in pharmaceutical sciences, chemistry, biology, biotechnology, or a related field.
• A minimum of 10 years of CMC development experience within the biopharmaceutical industry, with a demonstrated track record of leadership and successful cross-functional collaboration.
• Proven experience managing external manufacturing partners, including CMOs/CDMOs.
• Strong understanding of biologics development, GMP manufacturing, analytical development, and regulatory CMC requirements.
• Experience supporting clinical-stage programs and regulatory submissions.
• Strong project management, negotiation, communication, and problem-solving skills.
• Ability to work independently and effectively manage multiple programs in a fast-paced environment.
• Knowledge of regulatory requirements from CDE, FDA, and/or EMA.
• Experience leading CMC activities from early development through late-stage clinical programs.
• Excellent communication and negotiation skills, with fluency in spoken Mandarin and English highly preferred.

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html