Tech Transfer Operations Lead TTO (m/f/d), 80 - 100%

#Products #MedicalDevice # SecondaryPackaging #LeadProjects #TTO #21CRFpart 210/211 #ISO13485 #JetztBewerben #YourNewJob

Our customer, a pharmaceutical company based in Basel, needs reinforcement. For a temporary employment from 01.10.2026 to 30.09.2027 (1 year contract), we are looking for an experienced professional to support technical transfer operations.

Tech Transfer Operations Lead TTO (m/f/d), 80 - 100%

Benefits

• An internationally operating, innovative Swiss pharmaceutical company, a leader in its field
• Flexible working hours and extensive training opportunities
• A motivated multicultural team and environment

Your main responsibilities

• Responsible for technical transfer operations regarding combination products/medical device & secondary packaging implementation.
• Provide expertise from combination product/medical device platform point of view for strategical, process, technical, and esystems related topics during device development, commercialization and for commercial products.
• Establish and execute an aligned technical transfer strategy for GDPD with NTO and harmonizes cross-site manufacturing transfers from development to site level including alignment and upholding of template-based documentation for design transfers to NTO.
• Coordinate development support of product maintenance (LCM) for NTO as a customer and manage teams to implement changes concerning the medical device platform.
• Support but can also act as Transfer Team lead in Launch Site Decisions and in technical transfer and launch activities for assembly and packaging at involved sites and is member of the GDPD Device Development Sub Team.

Your Profile

• PhD, Dipl. Ing.. in Mechanical Engineering or Pharmaceutical Technology
• Fluent in English and local language. Other languages beneficial
• Minimum 5 years professional experience in Pharmaceutical Manufacturing (preferably assembly & packaging) / Manufacturing Science and Technology / technical Development in assembly & secondary packaging projects.
• Thorough understanding of product processes and strong working knowledge of applied statistics, quality systems and regulatory requirements across multiple health authorities.
• Fundamental understanding of standard device/packaging analytical testing.
• Expert in reviewing and writing technical reports.
• Strong Project management skills.
• Strong communication and intercultural skills with ability to work in a global matrix environment.

Jetzt bewerben