Tech Transfer Operations Lead
Flexsis AG, Filiale Basel LS
- 17.09.2026
- 100%
- Poste à responsabilités
- Temporaire
Tech Transfer Operations Lead
Description of the company
Flexsis is a company of the Interiman Group, one of the leading providers of personnel services in Switzerland. Thanks to our solid expertise as well as the competencies within the Interiman Group, we offer tailored solutions in personnel consulting.
For our client Novartis in Basel, we are looking for a reliable and motivated (m/f/d)
Tech Transfer Operations Lead
Duration: 1 year with extension possible
Workload: 80 - 100%
Role & Responsibilities- Lead technical transfers for combination products, medical devices, device assembly, and secondary packaging from development through commercial manufacturing.
- Develop and execute technical transfer strategies in collaboration with NTO and global cross-functional partners.
- Drive harmonization and standardization of manufacturing processes, technical approaches, and documentation across sites.
- Act as Technical Transfer Lead (TTL) for selected device and secondary packaging transfer and launch projects.
- Lead cross-functional project teams in a global matrix environment, partnering with Device Development, Manufacturing, TechOps, Regulatory, Quality, and Supply Chain.
- Bring your technical and manufacturing expertise into device development, commercialization, and product lifecycle management activities.
- Support design control and the development of robust, scalable assembly and packaging processes.
- A university degree, Master's or PhD in Mechanical Engineering, Pharmaceutical Technology, Manufacturing Engineering, Packaging Technology, or a related discipline.
- At least 5 years of relevant experience in pharmaceutical manufacturing, MS&T, technical development, or technical transfer, ideally within device assembly and secondary packaging.
- Solid expertise in combination products, medical devices, assembly, and packaging processes.
- Proven experience in technical transfer, commercialization, manufacturing implementation, and/or product lifecycle management.
- A strong understanding of quality systems, regulatory requirements, risk management, and applied statistics.
- Practical knowledge of design control and associated documentation, including DMR, DHF, pFMEA, Design Verification, and URS.
- Knowledge of relevant regulations and standards, including 21 CFR Parts 210/211, Part 4, Part 820, ISO 13485, ISTA, ASTM, and applicable European medical device requirements.
Have we sparked your interest and would you like to take your chance? Then we should definitely get to know each other! Simply click on "Apply now" and we look forward to receiving your complete application documents.