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Biologics specialization reduces competition, but Sun Pharma brand and generic manager title increase applicant density.
Role requires deep biologics and in-licensing experience, limiting transferability across industries.
Explicit 6–10 years industry experience, plus 2+ years PM and biologics expertise creates stringent filters.
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Own end-to-end program management for licensed and in-house biologics/biosimilars development including planning, budgeting, scheduling, and successful product launch.
Lead cross-functional teams (R&D, Regulatory, Manufacturing, Quality, Clinical, Commercial) ensuring alignment and execution of strategic objectives.
Manage external partner/licensor relationships for in-licensed products including governance, contractual obligations, and collaboration optimization.
Master’s degree in Life Sciences or MBA with relevant biopharma experience.
6–10 years biopharmaceutical industry experience with minimum 2 years in project/program management.
Experience in biologics/biosimilars domain including process development, manufacturing, or related functions.
Prior partner-facing, alliances, or in-licensing program management experience preferred but not mandatory.
Experienced in managing complex biologics or biosimilar development projects with multi-functional stakeholder coordination.
Comfortable acting as primary interface with external licensors and partners in regulated pharma environment.
Demonstrates strong program risk management and data-driven decision facilitation in cross-disciplinary contexts.