Mechanical Engineer Intern Zeltiq Aesthetics, Inc.
THIS JOB HAS EXPIRED Description
Assists in the design and development of medical device products from concept through production.
Essential Duties and Responsibilities include the following (other duties may be assigned.):
? Apply the principles of good drafting practice to all drawings of parts and assemblies
? Conceive, design, build, and evaluate prototypes to explore a range of design concepts.
? Under the guidance of technical leaders, create test plans and then execute the tests individually or with assistance from technicians or other engineers.
? Prepare, present, and document designs at reviews.
? Refine and develop selected concept(s) with oversight from manager or technical leaders.
? Work closely with other departments and outside entities, e.g. vendors and contract resources, to insure design and documentation conformance to all quality requirements
? Investigate and evaluate materials, adhesives, and assembly techniques with guidance from senior engineers or manager.
? Work with vendors, request quotes, prepare purchase orders.
? Create designs that follow best practices for manufacturability and assembly.
? Document ECO changes within Zeltiq Document Control.
? Manage the development of one or more part designs for a project design. Coordinate design constraints and resolves any design conflicts with assistance from manager or senior engineers.
Products under development are likely to include:
? Injection molded plastic parts
? Mechanical layout of flex circuits
? Elastomeric components
? Machined or sheet metal fabricated components
? Electrical connectors
? Pressure, force, and temperature sensors
? Individual must have strong verbal and written communication skills
? Proficient with 3D CAD software design tools for creating solid models, sheet metal parts, and drawings; strongly prefer experience with Creo (previously called Pro/E Wildfire).
? A minimum of two years education towards a BS Mechanical Engineering or equivalent degree.
? Individual will work under the general supervision of the manager or a technical leader.
? Under guidance from manager or technical leader, have the ability to set short term project goals and outline schedules for specific tasks.
? 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.
? 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