Senior Project Manager – Small Molecule Technology Transfers

The client is a leading organization in the pharmaceutical industry dedicated to the development and manufacturing of Small Molecule drug products. They prioritize innovation, quality, and regulatory compliance to deliver high-quality medicines to patients worldwide. We are seeking an experienced Senior Project Manager to lead and oversee large-scale Small Molecule drug product technology transfers across manufacturing sites. The role involves managing key projects from start to finish, ensuring timely complaints, and high-quality transfer execution to support the company's strategic growth.

Responsibilities: Lead multiple Small Molecule technology transfer projects, ensuring smooth site-to-site transfers; oversee project timelines, risks, and milestones via dashboards and reporting tools; collaborate closely with Manufacturing, Quality, Regulatory, Supply Chain, Procurement, and other teams to align project goals and resolve issues; develop and maintain project governance, provide best practices, and coach project teams and sponsors; act as the primary contact for manufacturing sites and global functions, fostering strong relationships and clear communication; support regulatory submissions related to transfers and ensure compliance with GMP standards; contribute to continuous improvement of transfer processes and methodologies, driving best practices across regions; provide technical expertise and support for resolving transfer-related challenges; perform additional duties as assigned by management.

Requirements: Bachelor’s degree or higher in Engineering, Chemistry, Biology, or a relevant scientific discipline; over 5+ years of experience in technology transfer, product development, or manufacturing operations within the pharmaceutical industry; extensive knowledge of Small Molecule drug product types, including liquids, ointments, creams, sterile injectables, and powders; proven ability to manage complex projects, with experience using enterprise project management tools like MS Project; strong knowledge of GMP regulations and regulatory processes, especially for EU and FDA standards; excellent stakeholder management, communication, and leadership skills; fluent in English, with additional language skills (e.g., German or French) considered an advantage; willingness to travel internationally approximately 10-20%.

If you are interested and want to apply, please submit your application via the apply button below and contact me.