Senior Engineer, Mechanical (Valencia (CA), United States)

Sonova AG

• $100K — $125K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or related discipline.
  • 5+ years in mechanical or microelectronic product development.
  • Experience with electromechanical product development from concept to manufacturing.
  • Skilled in designing miniature components and enclosures for electronic devices.
  • Knowledge of plastic-part design and injection molding processes.
  • Familiarity with biocompatibility requirements and materials like conductors and polymers.
  • Strong analytical and problem-solving abilities.

Responsibilities

  • Design and develop mechanical components for external and implantable systems.
  • Support product development from concept through to market introduction.
  • Establish mechanical specifications with cross-functional teams.
  • Create and update 3D CAD models and engineering documentation.
  • Apply design-for-manufacturing principles and methodologies.
  • Conduct design verification and validation testing activities.
  • Support sustaining engineering for existing products.

Benefits

  • Opportunity to work with innovative technology.
  • Collaborative work environment with talented colleagues.
  • Focus on making a difference in people's lives through technology.
Full Job Description
Valencia, California | Hybrid

In this role, you will support mechanical product-development activities throughout the complete lifecycle, including requirements development, design, prototyping, fabrication decisions, testing, verification, validation, failure analysis and sustaining engineering.

Responsibilities
  • Design and develop external and implantable systems and their associated mechanical components.
  • Support products from concept development through prototyping, manufacturing and market introduction.
  • Establish mechanical requirements and specifications in partnership with cross-functional teams.
  • Create and maintain 3D CAD models, engineering drawings, tolerance-stack analyses, design specifications and technical reports.
  • Apply design-for-manufacturing principles and established product-development methodologies.
  • Participate in make-versus-buy and fabrication decisions.
  • Ensure designs comply with functional requirements, internal procedures, quality-system requirements, industry standards and regulatory expectations.
  • Develop and execute design-of-experiments, component testing, product testing and verification and validation activities.
  • Conduct mechanical failure investigations and support root-cause analysis and corrective actions.
  • Support sustaining-engineering activities for existing products.
  • Prepare 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 regarding technical requirements, component development, tooling and manufacturing processes.
  • Work with consultants, vendors and members of the medical community.
  • Plan, coordinate and execute engineering assignments in support of project objectives.
  • Build knowledge of evolving clinical requirements, customer needs and product-use cases.
  • Collaborate effectively within multidisciplinary core teams.
  • Assist and mentor less-experienced engineering team members.
  • Perform other duties and responsibilities as assigned.


Qualifications
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering or a related engineering discipline.
  • Five or more years of mechanical or microelectronic product-development experience.
  • Experience developing electromechanical products from concept through manufacturing.
  • Experience designing miniature components, plastic and metal enclosures, microelectronic packages, connectors, cables, antennas, electrical contacts or switches.
  • Knowledge of plastic-part design, injection molding and manufacturing processes.
  • Knowledge of conductors, polymers, silicone, adhesives, coatings and biocompatibility requirements.
  • Experience creating 3D CAD models, engineering drawings and tolerance analyses.
  • Knowledge of product verification and validation, design controls and technical documentation.
  • Strong analytical, problem-solving and mechanical failure-analysis skills.
  • Strong communication, organization, teamwork and presentation skills.
  • Ability to coordinate across departments, manage priorities and meet project deadlines.
  • 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 $100,320-$125,400 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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