Technical Program Lead

Role: The position focuses on managing post-approval pharmaceutical projects, overseeing their scope, timelines, and milestones to ensure timely completion. Responsibilities include coordination across R&D, manufacturing, supply chain, regulatory, and business development teams; tracking material inventory, vendor qualification, validation activities, and submission schedules; and supporting cost-saving and alternative sourcing initiatives. The role also involves market intelligence, portfolio analysis, and evaluating new business opportunities. Qualifications: Bachelor's degree in a relevant field (Masters or MBA preferred), with a minimum of 5 years of pharma industry experience, particularly in generics. Proven management of projects and teams is required. High-Value: Emphasis on generic pharmaceuticals, post-approval lifecycle management, supply chain coordination, regulatory filings, and business development within the pharmaceutical industry. Work Setup: Not specified; details on location or travel are not provided.