Job Title

About the CompanyAt Biocon Biologics, we are creating a model for the future of healthcare for all. We are a leading company in the biosimilars revolution where patients come first. Our ambition is to impact a billion lives and we do this by fostering a culture of affordable innovation, patient centricity and disruptive thinking. We are a multicultural global company where employees have a purpose and passion to work closely with partners and patients. We have proven end to end expertise in the field of biosimilars, from its development, manufacturing, clinical development, regulatory approvals to commercialization. We have a long-term commitment to bring high quality affordable biosimilars to patients all over the globe.Key Responsibilities:Lead full lifecycle execution of medical device development programs, from concept through commercialization, in alignment with design control and regulatory standards.Own and manage program budgets, including financial forecasting, capital planning (CapEx), and monthly expense tracking.Collaborate with internal stakeholders (R&D, Regulatory, QA, Operations, SCM, Commercial, Legal) and external partners (OEMs, design houses, CROs) to drive progress across all workstreams.Maintain rigorous oversight of project timelines, critical path activities, and deliverables. Proactively identify risks and implement mitigation strategies.Facilitate partner interactions and serve as the primary point of contact for joint meetings, governance reviews, and strategic discussions.Review and assess RFQs (Requests for Quotation), ensure alignment with business and technical requirements, and obtain necessary internal approvals.Prepare and maintain program dashboards, trackers, and status reports; lead inter- and intra-departmental communications across global teams and plant-level functions.Champion continuous improvement in program governance, documentation, and project management systems.Technical / Functional Skills:Overall 8-10 years of experience in Medical device industry, minimum 5 years of project/program management experience preferably in drug delivery systems, or combination products.Strong knowledge of design control, device development processes, and lifecycle management.Proficiency in Microsoft Project, Excel, PowerPoint, and other project tracking tools.Experience working with global partners, cross-functional leadership, and plant-level operations.Background in mechanical or biomedical engineering is a plus (preferred but not mandatory).Behavioral / Leadership Skills:Strong stakeholder management and communication skills.Demonstrated ability to lead complex programs independently and drive cross-functional alignment.Strategic mindset with attention to detail, risk assessment, and execution discipline.Collaborative and adaptive team player with high accountability and ownership mindset.Note: This role will not be suitable for core IT Roles and the IT candidates will not be preferred for the role.