Manager - 2 Project Management

Sun Pharmaceutical Industries, Inc.; Vadodara; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Sun Pharmaceutical Industries Ltd invites applications for a Project Manager - In-Licensing to evaluate, acquire and manage pharmaceutical licensing opportunities. You will coordinate cross-functional activities from due diligence through filing, approval and commercialization, ensuring seamless integration of licensed products.

Responsibilities include leading due diligence with Regulatory, R&D, QMS, Supply Chain, Finance, BD and Legal teams; developing project plans; monitoring timelines and

Qualifications

• Experience evaluating in-licensing opportunities and managing cross-functional teams.
• Strong regulatory dossier understanding and lifecycle management.
• Ability to coordinate due diligence from evaluation to launch.

Responsibilities

• CFT Evaluation - Evaluate in-licensing opportunities aligned with business strategy
• Lead cross-functional due diligence involving Regulatory, R&D, Quality, Supply Chain, Commercial, Finance, Business Development and Legal teams.
• Assess dossier quality, manufacturing capabilities, intellectual property, regulatory pathways, and commercial viability.
• Identify risks and develop mitigation plans
• Drive consensus between partner’s technical teams and our CFT team.
• Develop and monitor project plans, timelines, budgets, and milestones.
• Coordinate activities from licensing agreement to product launch.
• Ensure timely execution of deliverables and stakeholder alignment.
• Weekly reporting of key ongoing projects
• Filing & approval monitoring of closed deals
• Act as the primary contact for licensors and external partners.
• Support execution of regulatory dossier submission as per country specific requirements.
• Build strong relationships to facilitate seamless collaboration.
• Coordinate dossier transfer, registration activities, and technology transfer.
• Support manufacturing readiness and launch planning.
• Monitor post-launch commitments and lifecycle management activities.
• Team working and stakeholder management.
• Working with external partner and internal R&D plant.
• Understanding of technical side and project complexities.

Skills

Project management

Cross-functional leadership

Regulatory affairs

Stakeholder management

Due diligence

Education

M.Pharm/MBA

Job description

Select how often (in days) to receive an alert: Create Alert

Company: Sun Pharmaceutical Industries Ltd

Job Title:

Business Unit:

R&D1 Regulatory Affairs

Job Grade

G11A

Location:

At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.

Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”

Job Description

The Project Manager - In-Licensing is responsible for evaluating, acquiring and managing pharmaceutical product licensing opportunities. The role coordinates cross-functional activities from due diligence through filing, approval and commercialization, ensuring successful integration of licensed products into the company's portfolio.

Key Responsibilities

• CFT Evaluation - Evaluate in-licensing opportunities aligned with business strategy
• Lead cross-functional due diligence involving Regulatory, R&D, Quality, Supply Chain, Commercial, Finance, Business Development and Legal teams.
• Assess dossier quality, manufacturing capabilities, intellectual property, regulatory pathways, and commercial viability.
• Identify risks and develop mitigation plans
• Drive consensus between partner’s technical teams and our CFT team.

Project Management

• Develop and monitor project plans, timelines, budgets, and milestones.
• Coordinate activities from licensing agreement to product launch.
• Ensure timely execution of deliverables and stakeholder alignment.
• Weekly reporting of key ongoing projects
• Filing & approval monitoring of closed deals

Partner & Alliance Management

• Act as the primary contact for licensors and external partners.
• Support execution of regulatory dossier submission as per country specific requirements.
• Build strong relationships to facilitate seamless collaboration.

Regulatory & Commercial Launch Support

• Coordinate dossier transfer, registration activities, and technology transfer.
• Support manufacturing readiness and launch planning.
• Monitor post-launch commitments and lifecycle management activities.
• Team working and stakeholder management.
• Working with external partner and internal R&D plant.
• Understanding of technical side and project complexities.

Key Performance Indicators (KPIs)

• On-time achievement of project milestones

NA

Job Requirements

Educational Qualification

M.Pharm/MBA

Experience

6-10 years of relevant experience

Your Success Matters to Us

At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together!

Disclaimer:

The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).