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The Project Manager will oversee cross-functional projects related to new product development, engineering changes, and operational improvements. This role focuses on executing initiatives that align with organizational goals while ensuring projects are completed on time, within scope, and within budget. This role reports to the Director - Project Management.

Support and manage projects related to product introductions, validation activities, contract manufacturing and facility upgrades, ensuring they are delivered within scope, budget, and timelines.
Support project planning and scheduling, while tracking progress and supporting timely resolution of issues.
Support project cost estimation and monitor project spending.
Work closely with R&D, Quality, Regulatory, Marketing and Manufacturing teams to ensure compliance with quality and regulatory processes.
Assist in preparing project documentation, risk assessments, and change controls, and provide regular updates to stakeholders.
Ensure all project activities meet the regulatory requirements.
Lead project meetings, provide regular status updates, project dashboards, and progress reports to stakeholders and leadership.

Technical Knowledge / Experience:
~ Bachelor’s degree in Engineering, Life Sciences, or related field.
~3–5 years of project management experience in a pharmaceutical, medical device, or biotechnology environment.
~ Solid understanding of GMP principles, validation protocols (IQ/OQ/PQ), and ECO/ECN (change control) processes.
~ Experience managing timelines, resources, and documentation in a regulated industry.
~ Proficiency with project management tools (MS Project, Smartsheet, Asana, or equivalent).
~ PMP certification or equivalent training preferred.


Detail-oriented with strong analytical and time-management abilities.
Demonstrates initiative, accountability, and commitment to quality outcome