Program Management Specialist

About the job

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 a 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.