Senior Expert Engineering (m/f/d) – Assembly & Molding for Medical Device
Job ID REQ-10054163
Summary
Location: Basel, Switzerland
Role 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 a 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 and novel drug delivery principles, e.g., drug delivery to the brain or radioligand therapy. We collaborate closely 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 produce state-of-the-art technical documentation for health authorities and production.
About the Role
Your Responsibilities:
* Develop platforms and collaborate with cross-functional teams to deliver safe, user-friendly, and reliable products.
* Lead and support teams in assembly and injection molding for device/part design, equipment, and process 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 the 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 of key regulations and standards (e.g., ISO 13485, ISO 23908, ISO 11608, ISO 10993, MDR, Design Controls).
* Ability to interact with cross-functional teams in a 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 accommodations to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process or to receive more detailed information about the essential functions of a position, please send an email to inclusion.switzerland@novartis.com, specifying your request and contact information. Please include the job requisition number in your message.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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