Job Description
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, o...
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, o...
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