New Product Development Program Lead

Location: Italy (Milan or Castelvecchio Pascoli)Kedrion Biopharma is strengthening its R&D pipeline of plasma-derived therapies to address high-unmet medical needs. We are seeking a talented New Product Development (NPD) Program Director / Director to lead Kedrion NPD strategic development platform — focusing on rare and orphan congenital protein deficiencies- driving end-to-end program execution from early development through market launch.This is a highly visible, global role responsible for aligning technical, clinical, regulatory, industrialization and commercial priorities to rapidly deliver impactful and innovative therapeutic solutions to patients worldwide.What You Will DoReporting to Global Operations Strategy Head, lead program planning and execution across the full product lifecycle — from pre-clinical to commercial ReadinessMatrix define and coordinate activities with Kedrion’s CR&IManage program governance, timelines, risks and milestone delivery in a matrixed, cross-functional environmentEnsure alignment with Global Operations strategy and business prioritiesDrive coordination across Regulatory, Clinical, R&I, Operations (R&D and manufacturing sites), Manufacturing Science and Development, Supply Chain, Quality, Marketing, Finance and HROversee overall program budget ensuring financial discipline and smart resource allocationAct as the “control tower” for monitoring performance and reporting to Senior Management (SteerCo, ExCom, S2PRC)Identify synergies, anticipate constraints and ensure proactive recovery actions where neededSupport industrialization scenarios and technology transfer planning for manufacturing scale-upPromote communication excellence, stakeholder alignment and execution disciplineRepresent the program in external collaborations, consulting engagements and business case evaluationsWhat You Bring (Required Experience & Sills)At least 5 years experience in Program/Project Management in biopharma (plasma-derived therapies is a plus)Proven track record in New Product Development: from pre-clinical / non-clinical to launch or BLA/MAA approval submission is preferredExperience in cross-functional global matrix organizations ― able to influence without authorityStrong understanding of product development in regulated environments (GxP, CMC, Phase progression, C>/biologics)Industry knowledge in plasma-derived therapies or rare disease biologics preferredDemonstrated ability to manage complex budget, governance and risk frameworksExcellent communication and presentation skills with Executive-level exposureProblem-solving mindset: able to connect strategy to execution and drive decisions quicklyFluent in English; Italian is a plusPhD in Life Sciences, Pharmacy or related fields — MBA or PMP certification is a plus;Summary: the candidate should hold a PhD in a relevant Biological Science (Biochemistry, Biotecechnology, etc.), have experience with the design, conduct and management of research (R&D, if possible) projects (preferably in an industrial context). Project management technical qualifications are welcome but not necessary, as relevant training will be provided. Strong communication and interpersonal skills (English and Italian), coupled with demonstrable negotiation skills and a results-oriented approach. Able to work to deadlines with minimal supervision in a complex, multidisciplinary environment.Who You Are (Key Competencies)Strategic thinker with structured execution disciplineExcellent communication and negotiation skills, strong focus on objectivesCollaborative leader who inspires trust and accountabilityComfortable handling ambiguity and evolving prioritiesInternational mindset and cultural agilityPassion for innovation and patient impactThis announcement is addressed to applicants of both sexes (L. 903/77 - D.Lgs n. 198/2006) and also to those belonging to Protected Categories (L.68/99).#J-18808-Ljbffr