Sr. Mechanical Engineer Zeltiq Aesthetics, Inc.
THIS JOB HAS EXPIRED Description
Title: Sr. Mechanical Engineer
Reports To: Mechanical Engineering Manager
Develops medical products from concept through production
Essential Duties and Responsibilities include the following (other duties may be assigned.):
? Completes layout and design of electronics packaging and fluidic system layout and packaging for a medical device.
? Conceive, design, build, and evaluate prototypes to explore a range of design concepts. Refine and develop selected concepts.
? Prepare, present, and document designs at reviews.
? Investigate and evaluate materials, adhesives, and assembly techniques.
? Manage vendors, request quotes, and prepare purchase orders.
? Perform pressure and flow analysis for fluidics systems.
? Plan, perform, and document verification testing.
? Interact with Clinical and Marketing departments to determine design requirements and goals.
? Design and validate packaging to ensure safe handling and transportation of devices.
? Document assembly procedures, and coordinate design transfer to manufacturing.
? Document ECO changes within Zeltiq Document Control process.
Other Duties and Responsibilities:
Products under development are likely to include:
? Injection molded plastic parts.
? Sheet metal enclosures including EMI mitigation.
? Large plastic enclosure panels and structural bases.
? Electrical connectors and cabling.
? Selection of pressure, flow, force, and temperature sensors
? Elastomeric components
? BS in Mechanical Engineering or equivalent degree.
? At least five years of product design and development experience required, ten years preferred.
? Prefer at least five years of experience in medical devices, ideally class II devices.
? Must be proficient with Pro/E Wildfire/Creo.
? Candidate should be a 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
? Must be familiar with the capabilities and limitations of a variety of fabrication techniques (e.g. plastic injection molding, vacuum and pressure forming, sheet metal, stamping, machining).
? 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.
||Pleasanton, CA |
THIS JOB HAS EXPIRED