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Sonova Group

Open 19d

Principal Engineer, Mechanical Design

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Summary

Principal mechanical engineer at Advanced Bionics (Sonova Group) leading the end-to-end mechanical design of cochlear implant and body-worn hearing devices — from requirements, 3D CAD and prototyping through verification, manufacturing and market launch — while mentoring engineers and ensuring FDA/ISO design-control compliance. Core tools include Creo/ProEngineer CAD, PLM/PDM and injection-molding

Valencia, California | Hybrid

Join Advanced Bionics, a Sonova Group company, as a Principal Mechanical Engineer and help develop innovative cochlear implant systems and body-worn medical devices that improve the lives of people with hearing loss.

In this role, you will provide technical leadership throughout the mechanical product-development lifecycle—from requirements and concept development through prototyping, verification, validation, manufacturing and market introduction. You will also mentor less-experienced engineers and collaborate with multidisciplinary teams, suppliers, consultants and members of the medical community.

Responsibilities

  • Lead the mechanical design and development of external and implantable systems and their associated components.

  • Develop products from initial concept through prototyping, manufacturing and commercial introduction.

  • Establish product requirements, technical specifications and mechanical design solutions.

  • Create and maintain 3D CAD models, engineering drawings, tolerance-stack analyses, design specifications and technical reports.

  • Apply design-for-manufacturing principles and structured product-development methodologies.

  • Lead make-versus-buy and fabrication decisions in collaboration with internal teams and external suppliers.

  • Ensure designs comply with functional requirements, internal procedures, quality-system requirements, industry standards and regulatory expectations.

  • Plan and support design-of-experiments, component testing, product testing and verification and validation activities.

  • Lead mechanical failure investigations and support root-cause analysis and corrective actions.

  • Support sustaining-engineering activities throughout the product lifecycle.

  • Establish and maintain Design History File documentation and participate in formal design reviews.

  • Ensure compliance with FDA and ISO design controls and documentation requirements.

  • Collaborate with suppliers on technical requirements, component development, tooling and manufacturing readiness.

  • Work with consultants, vendors and members of the medical and cochlear implant communities.

  • Provide technical guidance regarding technology partnerships, supplier relationships and intellectual property.

  • Plan, coordinate and execute engineering activities in support of project objectives.

  • Build and maintain knowledge of evolving clinical needs, product use cases and market requirements.

  • Mentor and coach engineers while providing cross-functional technical leadership within a core-team environment.

  • Perform other duties and responsibilities as assigned.

Qualifications

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering or a related engineering discipline.

  • Eight or more years of mechanical or microelectronic product-development experience.

  • Experience developing complex electromechanical products from concept through production.

  • Experience designing miniature mechanical components, plastic and metal enclosures, microelectronic packages, connectors, cables, antennas, electrical contacts or switches.

  • Knowledge of plastic-part design, injection molding, materials selection and manufacturing processes.

  • Knowledge of conductors, polymers, silicone, adhesives, coatings and biocompatibility requirements.

  • Experience creating 3D CAD models, engineering drawings and tolerance analyses.

  • Working knowledge of verification and validation, design controls and Design History File requirements.

  • Strong analytical, problem-solving and mechanical failure-analysis skills.

  • Demonstrated ability to lead technical work and mentor junior engineers.

  • Strong communication, organization, collaboration and presentation skills.

  • Ability to manage multiple priorities and meet project deadlines in a cross-functional environment.

  • Proficiency with Microsoft Office 365, PLM/PDM systems and ProEngineer/Creo or comparable CAD software, such as SolidWorks.

  • Ability to travel approximately 15%.

Preferred Qualifications

  • Master’s degree in Mechanical Engineering, Biomedical Engineering or a related field.

  • Medical-device product-development experience.

  • Experience with cochlear implants, hearing aids, wearable technology or consumer audio products.

  • Experience with finite element analysis, statistical analysis and Failure Mode and Effects Analysis.

  • Experience designing tooling and fixtures.

  • Experience using MS Project, Moldflow, ANSYS or Minitab.

Compensation

The target base salary range for this position is $131,560–$164,450 annually.

A career at Advanced Bionics offers an opportunity to work with innovative technology and collaborate with talented colleagues who share a commitment to helping people experience the joy of hearing.

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