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 solid 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 [email protected]

📌 Senior Manager Project Management & Business Development (Solapur)
🏢 Metina PharmConsulting
📍 Solapur