Senior Expert, Medical Device Eng – Autoinjector Systems

Novartis

Österreich

Vor Ort

EUR 67.000 - 118.000

Vollzeit

vor 29 Stunden
Sei unter den ersten Bewerbenden
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Benefits dieser Stelle

Performance bonus
Insurance plans
Retirement plans
Wellbeing resources
Global recognition programs
Hybrid working options
14 weeks parental leave

Zusammenfassung

Novartis is seeking a Senior Expert Engineering in Schaftenau, Austria, within the Global Device and Packaging Development (GDPD) team. You will lead technical development and lifecycle management for autoinjector devices and prefilled syringes, ensuring high quality and regulatory compliance in a cross-functional setting.

The role requires a engineering degree and 5+ years in medical device or combination products, with strong English skills and autonomy.

Qualifikationen

  • Bachelor, Master or PhD degree in engineering or equivalent.
  • Excellent English, verbal and written; German language skills are an advantage.
  • Autonomous and independent working style with interest in medical device development and lifecycle management.

Aufgaben

  • Deliver technical development and lifecycle management in cross-functional teams for easy-to-use, safe and robust products.
  • Responsible for device constituent parts of an autoinjector and system integration with prefilled syringes into a combination product.
  • Support device design development following the design control process and regulatory framework.
  • Ensure components are delivered and controlled to required quality for clinical trials and commercial production.
  • Support audits on medical devices and respond to health authority questions.

Kenntnisse

English proficiency

Ausbildung

Engineering degree (BSc/MSc/PhD)

Jobbeschreibung

Novartis is seeking a Senior Expert Engineering in Schaftenau, Austria, within the Global Device and Packaging Development (GDPD) team. You will lead technical development and lifecycle management for autoinjector devices and prefilled syringes, ensuring high quality and regulatory compliance in a cross-functional setting.

The role requires a engineering degree and 5+ years in medical device or combination products, with strong English skills and autonomy.

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