Program Management Specialist

Key Responsibilities:

• Manage and execute

  CDMO projects

  from initiation to delivery, ensuring adherence to timelines, budgets, and quality standards.
• Act as the

  primary point of contact

  for internal stakeholders, ensuring smooth communication and alignment on project objectives.
• Collaborate closely with the Site Head, R&D, Manufacturing, Quality, Supply Chain, and Regulatory teams to ensure project milestones are achieved.
• Monitor project progress, identify risks, and implement mitigation plans to ensure on-time and in-full delivery.
• Prepare and present regular status reports and updates to senior management.
• Drive process improvements to enhance project efficiency and client satisfaction.

Required Qualifications & Skills:

• Bachelor’s/Master’s degree

  in Life Sciences, Pharmacy, Chemical Engineering, or related field.

• 4-6 years

  of experience in managing projects in

  CDMO/Pharmaceutical

  companies is a must.
• Strong understanding of

  CDMO operations

  , including R&D, tech transfer, and manufacturing processes.
• Excellent stakeholder management, communication, and problem-solving skills.
• Ability to work in a fast-paced, matrixed environment with multiple internal teams.