Senior Expert Engineering – Medical Device Development

Position

Vollzeit

Senior

Ingenieurwesen

Konditionen

Basel (City)

Vor Ort

80–100%

Endet in 30 Tagen

Anforderungen

10+ J. Erfahrung

Bachelor

EU/EFTA-Bewilligung

Skills

Medical device developmentDesign for manufacturing and assemblyTolerance analysisMetrologyMaterial qualificationPrototypingComponent specification3D modelingDesign History File documentationRoot cause analysisCADProjektmanagement

Sprachen

Englisch C2

Beschreibung

Your responsibilities include, but are not limited to:

Work on platform device development and participate to project activities in cross-functional teams to deliver easy-to-use, safe and robust products
Contribute to the complete development process of medical devices: ideation, brainstorming, prototyping, piloting, manufacturing and complaint handling
Create and review IP
Work with CAD, 3D, drawings, tolerance analysis
Size and specify plastic and metallic components
Work with third party suppliers, including prototyper, tool makers, CMOs
Manage testing and characterization for acceptance, compliance, performance etc., and implement improvements
Perform root cause analysis and develop robust solutions to prevent re-occurrence
Ensure components are delivered and controlled to the required quality for clinical trials and commercial production
Author key design history file documents: design input requirements, component specifications and design verification documents.

Aufgaben

Work on platform device development and participate to project activities in cross-functional teams to deliver easy-to-use, safe and robust products
Contribute to the complete development process of medical devices: ideation, brainstorming, prototyping, piloting, manufacturing and complaint handling
Create and review IP
Work with CAD, 3D, drawings, tolerance analysis
Size and specify plastic and metallic components
Work with third party suppliers, including prototyper, tool makers, CMOs
Manage testing and characterization for acceptance, compliance, performance etc., and implement improvements
Perform root cause analysis and develop robust solutions to prevent re-occurrence
Ensure components are delivered and controlled to the required quality for clinical trials and commercial production
Author key design history file documents: design input requirements, component specifications and design verification documents.

Anforderungen

Degree in mechanical engineering or equivalent
Preferably 10 years of experience in medical device development
Proficient oral communication and excellent technical writing skills in English is a must
Experience in designing plastic and metal components; tolerance analysis; metrology; lab testing
Experience in material qualification
Good knowledge in design for manufacturing and assembly
Good knowledge of key regulations and standards
Track record in Design History File documentation
Ability to interact with cross functional team in matrix organization

Technologien

CAD3Dtolerance analysis

Vorteile

Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.
Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals.

Unternehmen

Novartis

Pharmaceuticals

At Novartis, we are reimagining medicine to improve and extend people's lives. We discover and develop breakthrough treatments and find new ways to bring cures to as many people as possible. Without safe, easy-to-use, high-quality drug delivery devices our patients could not get their medicines.

Kontakt

inclusion.switzerland@novartis.com