Production Assembler Zeltiq Aesthetics, Inc.
THIS JOB HAS EXPIRED Description
The Production Assembler is responsible for the assembly/build of Zeltiq products that meet product quality requirements and Customer shipment deadlines.
Essential Duties and Responsibilities include the following (other duties may be assigned.):
? Performs electro-mechanical assembly of final products, sub-assemblies and related medical device products by following released procedures
? Employs high standards of workmanship to ensure high quality products are produced on schedule. Typically works on assignments under the guidance of a senior assembler or lead.
? Makes recommendations for improvement of production methods and product design issues
? Relies on instructions and pre-established guidelines to perform the functions of the job.
? Must be able to work in a team oriented atmosphere with assemblers, technicians, QA personnel, and engineers, completing tasks and communicating effectively, both orally and in writing.
? Performs in-process inspection to ensure products meet specifications and standards.
? Generates required documentation to complete the Device History Record (DHR).
? May require engineering support to resolve complex and unique problems.
? Must be able to read and understand: assembly instructions, production orders, Bills of Materials, Standard Operation Procedures, and all other documentation used to control the products and processes.
? Confers with engineers, technicians, production personnel, and others regarding assembly procedures.
? Will provide support to project teams whose objectives may be: quality improvement, cost reduction, cycle time reduction, reliability improvement, increased operational efficiency, or new product introduction.
? Assists in creating and updating process and product documentation.
? Collaborates with peers to achieve shared departmental goals.
? Keeps work area clean, organized, and safe.
? Fills out time sheets and all other required paperwork accurately and on time.
? Other duties may be assigned.
? Must be available to work overtime as requested by the supervisor. This may include nights, weekends, and holidays during times critical to our business such as month-end, quarter-end, and year-end
? High School diploma or equivalent.
? 0 to 3 years of work experience.
? Ability to effectively communicate information and respond to questions both verbally and in writing.
? Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 25 lbs on a daily basis
? PC user, familiar with Word, Excel, and Windows
? Must be willing to be trained in other areas of production
? Knowledge and adherence to safety procedures and programs
? 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