About this role
This role is responsible for managing and executing post-approval pharmaceutical projects from initiation through commercial implementation, including project timelines, material readiness, method validation/verification, submission batches, stability, regulatory filings, approvals, and cross-functional coordination. The position also supports strategic portfolio management and business development by evaluating alternate-source and cost-saving opportunities, analyzing market and regulatory factors, developing financial models, and partnering with Supply Chain, Operations, Regulatory Affairs, R&D, and other stakeholders to ensure projects align with business objectives.