Global Technical Transfer Lead - Medical Devices

Job-Room

Basel

Vor Ort

CHF 120.000 - 190.000

Teilzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Zusammenfassung

Job-Room in Basel seeks a Technical Transfer Manager – Medical Devices (m/f/d) for 80-100% capacity on a temporary assignment (01.10.2026 – 30.09.2027). Lead technical transfer projects for combination products and devices across an international manufacturing network, driving transfer strategies and coordinating cross-functional teams.

Ideal candidates hold a PhD or engineering degree with several years in pharmaceutical manufacturing, knowledge of DHF/DMR/pFMEA, regulatory frameworks (ISO

Qualifikationen

  • Completed studies in Mechanical Engineering, Pharmaceutical Technology or related field.
  • Several years of experience in pharmaceutical manufacturing, assembly or packaging.
  • Experience with design controls (DHF/DMR/pFMEA) and regulatory knowledge.

Aufgaben

  • Lead technical transfer projects for medical devices and combination products.
  • Define transfer strategy linking development with site operations.
  • Act as Transfer Team Lead for device launches across networks.
  • Support lifecycle management and device platform changes.
  • Collaborate with Device Development, Regulatory Affairs and Supply Chain.
  • Contribute to audits covering packaging and medical device topics.
  • Prepare technical documentation for registrations and regulatory questions.

Kenntnisse

Mech Eng
Pharma Tech
Transfer Mgmt
PM & Analytics
Cross-functional
Regulatory Awareness

Ausbildung

PhD or Eng Degree

Jobbeschreibung

Job-Room in Basel seeks a Technical Transfer Manager – Medical Devices (m/f/d) for 80-100% capacity on a temporary assignment (01.10.2026 – 30.09.2027). Lead technical transfer projects for combination products and devices across an international manufacturing network, driving transfer strategies and coordinating cross-functional teams.

Ideal candidates hold a PhD or engineering degree with several years in pharmaceutical manufacturing, knowledge of DHF/DMR/pFMEA, regulatory frameworks (ISO

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