Arevna is supporting a growing medical device company in their search for a Senior Development Engineer to drive product innovation from concept to commercial launch. This role offers the opportunity to work on a range of devices, ensuring technical excellence, regulatory compliance, and successful market introduction.
If you want to know about the requirements for this role, read on for all the relevant information.
Must have background within implantable devices - No sponsorship available.
Key Responsibilities:
* Lead product development projects, from line extensions to complete device systems
* Refine designs for technical, clinical, and commercial feasibility
* Develop technical documentation in compliance with FDA, ISO 13485, and MDR requirements
* Oversee risk management and design verification/validation testing
* Support regulatory submissions, including 510(k) filings
What We’re Looking For:
* Degree in engineering or a related field
* 5+ years’ experience in medical device development
* Strong proficiency in 3D CAD (Siemens NX preferred)
* Knowledge of quality systems (ISO 13485, 21 CFR 820)
If you're looking for a role where you can contribute to innovative medical technologies, we’d love to hear from you. Get in touch to learn more.