Senior Project Manager - Small Molecule Technology Transfers

Company
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.

Job Description
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%.

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

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