JOB DETAILS

Senior Expert Engineering – Medical Device Development

CompanyNovartis
LocationBasel
Work ModeOn Site
PostedJune 15, 2026
About The Company
Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide. Find out more at https://www.novartis.com See our community guidelines: https://go.novartis.social/3Nboxki
About the Role

Job Description Summary

Location: Basel, Switzerland #onsite

Role Purpose:
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. This is where you come in, the Device Technology Solution Center is looking for a Senior Design Engineer for the development of drug device combination products.

The aim is to develop a new auto-injector platform from early phase development to market launch.


 

Job Description

Your Responsibilities:

 

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.

 

Role Requirements

 

  • 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
  • Minimum 80% on site work – 4 days/week

 

 

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. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
 


 

Skills Desired

Key Skills
Medical Device DevelopmentCAD3D ModelingTolerance AnalysisDesign for Manufacturing and AssemblyDesign History File DocumentationRoot Cause AnalysisMaterial QualificationMetrologyLab TestingTechnical WritingCross-functional Team Collaboration
Categories
EngineeringHealthcareManufacturingScience & Research
Job Information
📋Core Responsibilities
Lead the development of a new auto-injector platform from early phase to market launch within a cross-functional team. Manage the complete device lifecycle including ideation, prototyping, manufacturing, and design verification documentation.
📋Job Type
full time
📊Experience Level
10+
💼Company Size
82768
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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