Tech Transfer Operations Lead TTO
Job in
4040, Basel, Kanton Basel-Landschaft, Switzerland
Listed on 2026-09-24
Listing for:
EDP Personalberatung GmbH
Seasonal/Temporary
position Listed on 2026-09-24
Job specializations:
-
Engineering
Quality Engineering, Medical Device Industry, Biomedical Engineer, Manufacturing Engineer
Job Description & How to Apply Below
Tech Transfer Operations Lead TTO (m/f/d), 80 - 100%
#Products #Medical Device # Secondary Packaging #Lead Projects #TTO #21
CRFpart 210/211 #ISO
13485 #Jetzt Bewerben #Your New Job
Our customer, a pharmaceutical company based in Basel
, needs reinforcement. For a temporary employment from to (1 year contract), we are looking for an experienced professional to support technical transfer operations.
- 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
- 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.
- 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.
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