Assistant General Manager - R&D Project Management

We are seeking an experienced and proactive

Project Manager

to lead the end-to-end execution of pharmaceutical development and commercialization projects, specifically for

Solid Oral Dosage Forms and Liquid Orals . The selected candidate will manage cross-functional coordination from

product development, technology transfer, regulatory filing to Approvals , ensuring all project milestones are delivered on time, within scope, and in full compliance with business and regulatory requirements.

Skills and Competencies :

Deep understanding of

pharmaceutical product development, technology transfer &

Familiarity with global

regulatory frameworks and dossier submission processes

Strong competency in

project planning, risk management, and cross-functional leadership .

Proficiency in

Microsoft Project, Excel and PowerPoint

for real-time project tracking and reporting.

Excellent

stakeholder management, communication, negotiation and leadership skills .

Highly

organized, proactive and solution-focused

approach to project management.

Key Attributes : Collaborative and

team-oriented leadership style .

Strong

analytical thinking and problem-solving

capabilities.

Ability to perform effectively under

tight deadlines in a regulatory-compliant environment .

High degree of

ownership, accountability, and customer-centric mindset .

Key Responsibilities :

Lead the

planning, execution, and delivery

of pharmaceutical projects — encompassing Formulation Development, Analytical Development, Regulatory Filing, Manufacturing, and Supply Chain — from initiation through Product Approval.

Develop and maintain

comprehensive project plans

including timelines, milestones, resource allocation and risk mitigation strategies using standard project management tools.

Coordinate

cross-functional teams

including R&D, Regulatory Affairs, Quality Assurance, Production, Supply Chain, and Business Development to ensure effective collaboration and timely execution.

Manage

technology transfer activities

from R&D to manufacturing, ensuring robust scale-up, validation, and readiness for commercial production.

Serve as the

central communication point

for internal teams and external partners, ensuring alignment on project goals, timelines, and deliverables.

Ensure

regulatory submission preparedness

for assigned projects and provide active support during

dossier filing and query resolution

for designated markets.

Identify potential risks, establish

risk mitigation strategies , and ensure early resolution to maintain project timelines and objectives.

Monitor

project budgets and resource allocations

to ensure optimal utilization, escalating deviations where necessary to maintain alignment with organizational goals.

Organize and facilitate regular

project review meetings ; prepare clear, data-driven

status reports and dashboards

for senior management.

Ensure strict compliance with

GMP, global regulatory guidelines (USFDA, EMA, WHO, MHRA, etc.) , and internal quality standards throughout the project lifecycle.

Experience required 17 to 20 years