Proclinical is collaborating with a pharmaceutical company to find a dedicated and performance-oriented individual for a lead position in External Manufacturing Operations. This exciting role offers the opportunity to join a dynamic department.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
Lead the operational management of Contract Development and Manufacturing Organizations (CDMOs) and vendors.
Serve as the primary contact for CDMO/vendor management, including relationship management and business support.
Lead cross-functional vendor teams to ensure continuous supply of compliant products and services.
Manage projects and programs from early phase development to commercialization, including new product introductions and lifecycle management.
Provide technical support to affiliate teams overseeing local CMOs.
Support due diligence activities and implement industrial manufacturing strategies for local and global CDMOs.
Represent the External Manufacturing Team in transversal project and improvement programs.
Key Skills and Requirements:
Master's degree in a relevant field.
Significant operations management experience in a GMP environment, particularly in drug product and device manufacturing.
Experience in pharmaceutical project management.
Strong technical knowledge of pharmaceutical manufacturing.
Familiarity with regulatory requirements and best practices to ensure compliance and drive improvements.
Fluency in English. French would be highly desirable.
Ability to lead multi-functional teams, manage complex projects, and influence external business partners to deliver results.
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