Hiring for Sr.Manager/AGM-Project Management (CDMO) API

Key Responsibilities:Manage multiple CDMO projects from start to finish. Act as the main contact for Big Pharma clients, ensuring smooth communication. Work with R&D, manufacturing, QA/QC, regulatory, and supply chain teams to meet project goals. Plan project timelines, track progress, and resolve issues. Oversee project costs, budgets, and profitability from a techno-commercial perspective. Support proposal preparation, quotations, and technical-commercial discussions. Ensure compliance with GMP, regulatory, and quality standards. Identify risks and implement solutions to keep projects on track. Experience managing Big Pharma or global clients. Strong techno-commercial knowledge (technical + business understanding). Good understanding of pharmaceutical processes, regulatory requirements, and quality standards. Strong communication, leadership, and coordination skills. Qualifications & Experience:Ph.D. in Pharmaceutical Sciences, Chemistry, or related field. 12–20 years of experience in project management in CDMO, CRAMS, or pharmaceutical manufacturing.