Senior Expert Engineering (m/f/d) â Assembly & Molding for Medical Device
Senior Expert Engineering (m/f/d) â Assembly & Molding for Medical Device
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1 Vacancy
Job Description
Job Description Summary
Location: Basel SwitzerlandRole Purpose:
Without safe easy-to-use high-quality drug delivery systems our patients could not get their medicines. This is where you come in; the Device Technology Solution Center needs you as Senior Expert Engineering for the development of drug device combination products working alongside our talented bright and diverse teams.
Our Device Technology Solution Center drives the technical development of auto-injectors as well as novel drug delivery principles e.g. drug delivery to the brain or radioligand therapy. We closely collaborate with project management human factors engineers packaging experts analytical testing production external partners regulatory experts and many more.
The aim is to develop and/or integrate innovative drug delivery systems with drug formulation and author state-of-the-art technical documentation for health authorities and production.
Job Description
Your Responsibilities:
Your responsibilities include but are not limited to:
Develop platforms and collaborate with cross-functional teams to deliver safe user-friendly and reliable products
Lead and support teams in the field of assembly and injection molding for device/part design equipment and process across from prototyping to commercial scale
Create and maintain relevant Design History File (DHF) documents ensuring high-quality device design and development
Contribute to all phases of medical device development: ideation prototyping piloting and manufacturing transfer
Ensure components meet quality standards for clinical trials and commercial production
Collaborate with external partners including prototypers toolmakers and CMOs
Identify root causes of issues define and implement robust solutions
Role Requirements
Degree in mechanical engineering or equivalent
Preferably 10 years of experience in medical device development
Proficient spoken communication and excellent technical writing skills in English
Proven experience in production of plastic and metal components
Proven experience in assembly of plastic and metal components / sub-assemblies
Proven experience in design for manufacturing and design for assembly
Good knowledge in key regulations and standards (e.g. ISO 13485 ISO 23908 ISO 11608 ISO 10993 MDR Design Controls)
Ability to interact with cross functional team in matrix organization
Commitment to Diversity and 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 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Skills Desired
Required Experience:
Senior IC
Employment Type
Full-Time
