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Future Opportunities - Join Our Talent Pipeline for R&D Device Engineer – Mechanical, Electrical, or Software Engineer

AbbVie

Salary not specified
Aug 30, 2025
Pleasanton, CA, US
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Allergan Aesthetics is looking to build a talent pipeline for future Device Engineer roles to design and develop medical products from initial concept through transfer to production.

Requirements

  • Skills for thermal or structural analysis as well as statistical analysis are needed.
  • Proficient with basic standard concepts and constraints involved in creating new product designs.
  • Should be knowledgeable of new modern methods for making prototype or production parts.
  • Ability to set medium term project goals and outline schedules for multiple tasks for several team members.

Responsibilities

  • Act as a technical lead for product development projects.
  • Manage the overall development of parts and subassemblies for a project design.
  • Conceive, design, build, and evaluate prototypes to explore a range of design concepts.
  • Prepare, present, and document designs at technical reviews.
  • Investigate and evaluate materials, adhesives, and assembly techniques based product requirements and based on past experience.
  • Use best methods of design for manufacture and assembly (DFMA) and document the DFMA benefits of the chosen design.
  • Plan, perform, and document verification testing.

Other

  • BS in Mechanical, Software, Electrical Engineering or equivalent degree. Advanced degree desirable.
  • Must have at least eight years of product design and development experience; prefer ten years of experience.
  • Prefer at least three years of experience in medical devices, ideally class II devices.
  • Individual will complete work with minimal supervision of the manager.
  • Strong team player with the demonstrated abilities and willingness to wear “multiple hats” and perform a wide range of tasks within a dynamic environment.
  • Individual must have strong verbal and written communication skills.
  • Responsible for performing all duties in compliance with FDA’s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies.