Global Program Management- Devices

About the Company

At 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:

1. Lead full lifecycle execution of

   medical device development programs

   , from concept through commercialization, in alignment with design control and regulatory standards.
2. Own and manage

   program budgets

   , including financial forecasting, capital planning (CapEx), and monthly expense tracking.
3. 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.
4. Maintain rigorous oversight of

   project timelines, critical path activities

   , and deliverables. Proactively identify risks and implement mitigation strategies.
5. Facilitate partner interactions and serve as the

   primary point of contact

   for joint meetings, governance reviews, and strategic discussions.
6. Review and assess

   RFQs (Requests for Quotation)

   , ensure alignment with business and technical requirements, and obtain necessary internal approvals.
7. Prepare and maintain

   program dashboards, trackers, and status reports

   ; lead inter- and intra-departmental communications across global teams and plant-level functions.
8. 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.