Sr.Manager/AGM-Project Management

As a Senior Manager / AGM/DGM Project Management in the Project Management / Contract Development & Manufacturing Organisation (CDMO) department located in Hyderabad, your role overview includes managing multiple CDMO projects from initiation to completion. You will serve as the primary point of contact for Big Pharma clients, ensuring effective communication throughout the project. Collaboration with R&D, manufacturing, QA/QC, regulatory, and supply chain teams will be essential to achieve project objectives. Your responsibilities will also involve planning project timelines, monitoring progress, and resolving any issues that arise. Additionally, you will oversee project costs, budgets, and profitability from a techno-commercial perspective. Supporting proposal preparation, quotations, and engaging in technical-commercial discussions will be part of your duties. Compliance with GMP, regulatory, and quality standards is crucial, and you will be expected to identify risks and implement solutions to ensure project success.

Key Responsibilities: - Manage multiple CDMO projects, ensuring successful delivery. - Act as the main point of contact for Big Pharma clients to facilitate smooth communication. - Collaborate with various teams to achieve project goals effectively. - Plan project timelines, monitor progress, and address any issues promptly. - Oversee project costs, budgets, and profitability with a techno-commercial focus. - Support in proposal preparation, quotations, and engage in technical-commercial discussions. - Ensure compliance with GMP, regulatory, and quality standards. - Identify risks and implement solutions to maintain project timelines.

Qualifications Required: - Ph.D. in Pharmaceutical Sciences, Chemistry, or related field. - 12 to 15 years of experience in project management within CDMO, CRAMS, or pharmaceutical manufacturing. - Experience managing Big Pharma or global clients. - Strong techno-commercial knowledge with a solid grasp of technical business understanding. - Good understanding of pharmaceutical processes, regulatory requirements, and quality standards. - Excellent communication, leadership, and coordination skills.

In addition to the above, the company values individuals who bring a wealth of experience in project management within the pharmaceutical industry and are adept at handling complex projects involving Big Pharma or global clients. As a Senior Manager / AGM/DGM Project Management in the Project Management / Contract Development & Manufacturing Organisation (CDMO) department located in Hyderabad, your role overview includes managing multiple CDMO projects from initiation to completion. You will serve as the primary point of contact for Big Pharma clients, ensuring effective communication throughout the project. Collaboration with R&D, manufacturing, QA/QC, regulatory, and supply chain teams will be essential to achieve project objectives. Your responsibilities will also involve planning project timelines, monitoring progress, and resolving any issues that arise. Additionally, you will oversee project costs, budgets, and profitability from a techno-commercial perspective. Supporting proposal preparation, quotations, and engaging in technical-commercial discussions will be part of your duties. Compliance with GMP, regulatory, and quality standards is crucial, and you will be expected to identify risks and implement solutions to ensure project success.

Key Responsibilities: - Manage multiple CDMO projects, ensuring successful delivery. - Act as the main point of contact for Big Pharma clients to facilitate smooth communication. - Collaborate with various teams to achieve project goals effectively. - Plan project timelines, monitor progress, and address any issues promptly. - Oversee project costs, budgets, and profitability with a techno-commercial focus. - Support in proposal preparation, quotations, and engage in technical-commercial discussions. - Ensure compliance with GMP, regulatory, and quality standards. - Identify risks and implement solutions to maintain project timelines.

Qualifications Required: - Ph.D. in Pharmaceutical Sciences, Chemistry, or related field. - 12 to 15 years of experience in project management within CDMO, CRAMS, or pharmaceutical manufacturing. - Experience managing Big Pharma or global clients. - Strong techno-commercial knowledge with a solid grasp of technical business understanding. - Good understanding of pharmaceutical processes, regulatory requirements, and quality standards. - Excellent communication, leadership, and coordination skills.

In addition to the above, the company values individuals who bring a wealth of experience in project management within the pharmaceutical industry and are adept at handling complex projects involving Big Pharma or global clients.