Senior Manager Project Management & Business Development

Metina PharmConsulting Pvt. Ltd. · India

Job Description

Role: Senior Manager Project Management & Business Development

Experience: 8 to 10 Years

Industry: Pharmaceutical Consulting (GMP & Regulatory Affairs)

Location: Navi Mumbai (with travel as required)

Company Information

We are a reputed Pharmaceutical Consulting firm specializing in GMP and Global Regulatory Affairs. Headquartered in Navi Mumbai, with subsidiaries in Singapore, Australia, Europe, and Malaysia, we provide high-quality and committed consulting services to the pharmaceutical industry in India and internationally. We have a young, dynamic, and dedicated team of GMP and Regulatory experts and offer an entrepreneurial environment with strong learning and growth opportunities.

Role Overview

Techno-Commercial Project Management professional with 8 to 10 years of experience in the pharmaceutical industry to lead cross-functional product development and supply project execution while ensuring commercial viability and technical excellence. The role requires strong project management capabilities combined with a sound understanding of pharmaceutical regulatory, quality, manufacturing, product development, and commercial operations.

The ideal candidate will coordinate multiple stakeholders including Business Development, Regulatory Affairs, Quality Assurance, Manufacturing, R&D, Supply Chain, Finance, and clients to ensure successful execution of pharmaceutical consulting and regulatory projects.

Key Roles & Responsibilities

· Lead end-to-end execution of pharmaceutical product development , ensuring delivery within scope, timeline, budget, and quality standards.

· Develop project plans, monitor progress, manage risks, and optimize resource utilization.

· Coordinate cross-functional teams including Business Development, Regulatory Affairs, Quality, Manufacturing, R&D, Supply Chain, and Finance.

· Support business development through technical evaluations, commercial proposal preparation and closing license and supply agreements with CMOs and other business partners

· Manage client relationships with CMOs/ CROs/ Marketing partners , conduct project review meetings, and ensure high customer satisfaction.

· Ensure compliance with global regulatory requirements, GMP, and applicable quality standards.

· Oversee project budgets, profitability, contract compliance, and financial performance.

· Establish PMO governance, maintain project dashboards, KPIs, and management reports.

· Support strategic initiatives, portfolio planning, and organizational growth.

· Represent the organization in client meetings, audits, and business engagements as required.

· Travel for client meetings, audits, or conferences (domestic/international) as required.

Experience & Qualifications

· Graduate or Post Graduate degree in Pharmaceutical Sciences.

· Around 8-10 years of experience in pharmaceutical product lifecycle management, regulatory, product development, or consulting environment.

· Exposure to project management activities in pharmaceuticals

· Understanding of project financial tracking and timelines.

· Strong communication and coordination skills.

· Good time management skills with ability to handle multiple tasks and deadlines.

· High attention to detail, accuracy, and diligence.

Mail your resume at info@metinapharmconsulting.com