Vice President, Chemistry, Manufacturing & Controls (CMC)

Skills at this level

CMC Regulatory Submission Management

— Manages execution of CMC documentation including IND, IMPD, CTA, NDA, BLA, post-approval supplements, annual reports and registration renewals, and authors responses to health-authority questions.

Phase-Appropriate CMC Strategy

— Develops and executes global product and project regulatory strategies with robust assessment of global CMC requirements matched to the product's stage of development.

Regulatory Success Risk Assessment

— Assesses the probability of regulatory success for a product and defines the risk-mitigation measures needed to secure regulatory milestones through development.

Analytical Method Life Cycle Management

— Owns method remediation, validation, transfer, troubleshooting and OOT/OOS investigations along with data trending analysis for late-stage and commercial methods.

Technology Transfer & Manufacturing Readiness

— Directs transfer of processes and methods into manufacturing and ensures CMC documentation and processes are ready to support production at scale.

External Manufacturing Partner Management

— Selects and governs contract manufacturers and vendors, managing them to deliver CMC deliverables and maintain product integrity across the drug-development process.

Health Authority Negotiation

— Represents the organization's CMC positions to regulatory agencies, negotiating critical technical and compliance matters and defending the chemistry and manufacturing story.

Global CMC Compliance & Audit Oversight

— Sets and maintains large-scale manufacturing compliance posture and directs compliance audits so that CMC practices meet evolving regulator expectations across regions.

CMC Product Leadership

— Serves as accountable lead for a product's entire CMC regulatory destiny, coordinating delivery of all regulatory milestones through development and into commercialization.

Cross-Functional CMC Integration

— Aligns regulatory affairs, quality assurance, analytical development and manufacturing to ensure product integrity and coherent CMC deliverables throughout drug development.

Technical Authority & Mentorship

— Acts as scientific and technical authority within and across CMC functions, guiding local, regional and global associates so development and regulatory strategies stay current.

Corporate CMC Policy Development

— Drives company-wide CMC policies and regulatory-negotiation standards that define how subordinate development, analytical and manufacturing functions operate.