Senior Expert Engineer: Medical Devices & Combination Products

Novartis; Österreich; Vor Ort; EUR 67.000 - 118.000; Vollzeit

Benefits dieser Stelle

Flexible work model

Parental leave

Insurance plans

Wellbeing resources

Global recognition

Zusammenfassung

Novartis in Schaftenau, Austria, seeks a Senior Expert Engineering to lead development of parenteral combination products within the GDPD. You will drive device components, system integration with autoinjectors and prefilled syringes, and ensure timely delivery of technical aspects across projects.

The role emphasizes design control, regulatory alignment, and lifecycle management, collaborating with cross-functional teams to meet quality for trials and commercial production.

Qualifikationen

• Bachelor, Master or PhD in engineering or equivalent.
• 5+ years in medical device and/or combination product development.
• Experience with plastic and metal components; tolerance analysis, modelling and testing.
• Excellent English; German language skills are an advantage.
• Autonomous and independent work style in medical device development and lifecyle management.
• Ability to interact with cross-functional teams in a matrix organization.

Aufgaben

• Deliver technical development and lifecycle management in cross-functional teams for easy-to-use, safe and robust products.
• Responsible for device components of an autoinjector and integration with prefilled syringes into a combo product.
• Support device design development following design control processes and regulatory frameworks.
• Ensure components are delivered to required quality for clinical trials and production.
• Support internal and external audits on medical devices and respond to health authority questions.

Kenntnisse

English proficiency

German advantage

Cross-functional collaboration

Autonomous working

Ausbildung

Engineering degree (BSc/MSc/PhD)

Jobbeschreibung

Novartis in Schaftenau, Austria, seeks a Senior Expert Engineering to lead development of parenteral combination products within the GDPD. You will drive device components, system integration with autoinjectors and prefilled syringes, and ensure timely delivery of technical aspects across projects.

The role emphasizes design control, regulatory alignment, and lifecycle management, collaborating with cross-functional teams to meet quality for trials and commercial production.