Job Description

Job Purpose

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To manage end-to-end project completion for Injectable and Ophthalmic products, ensuring timely development, technology transfer, regulatory filings, validation, and commercial launches through effective cross-functional coordination to meet client expectations.

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Key Responsibilities

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Lead project planning, execution, monitoring, closure, and source change management activities.
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Coordinate with R&D;, Manufacturing, QA, QC, Regulatory Affairs, Engineering, Supply Chain, and Commercial teams for successful project delivery.
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Drive technology transfer, scale-up, validation, and commercialization of products for US and other regulated markets.
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Ensure achievement of project milestones and maintain OTIF (On-Time-In-Full) performance above 95%.
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Monitor project timelines, identify risks, and implement mitigation plans to ensure timely execution.
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Conduct project review meetings and provide timely progress updates to management and customers.
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Manage client projects and meeting expectations to partner them as a CMOs,



and CDMOs.
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Ensure compliance with GMP requirements, regulatory commitments, quality standards, and customer agreements.
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Drive validation, and commercialization targets aligned with business objectives.
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Escalate critical project and resource issues in a timely manner and drive resolution through cross-functional collaboration.
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Qualification & Experience

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M. Pharm / Masters in PMP
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8–12 years of experience in Project Management, Technology Transfer, Product Development, or Operations in Injectable/Ophthalmic formulations.
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Experience in managing projects for USFDA and other regulated markets.
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Key Competencies

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Project Management
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Technology Transfer
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Stakeholder Management
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Risk Management
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Regulatory & GMP Compliance
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Leadership & Team Management
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Communication & Problem Solving
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📌 Manager Project Management Chamba
🏢 Immacule Lifesciences
📍 Chamba