Job Details

ID #20830081
State California
City San diego
Job type Contract
Salary USD $Based on Experience Based on Experience
Source Stellar Consulting Solutions
Showed 2021-10-08
Date 2021-10-07
Deadline 2021-12-05
Category Et cetera
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Quality Engineer - Medical Devices - San Diego, CA

California, San diego, 92108 San diego USA

Vacancy expired!

Stellar Consulting Solutions is a boutique business & technology consulting company headquartered in Atlanta, GA. We deliver high quality, agile, and experienced workforce for niche technology projects of any scale. We help forward thinking clients to solve specific problems by understanding their needs and align talent that can move fluidly to match skill supply and demand on a real-time basis. Stellar Consulting has a unique combination of technical and digital skills to recruit, engage, and retain qualified talent. We have a stellar reputation for striving to achieve high ethical standards. Our use of Innovative techniques and industry best practices has made us one of the fastest growing boutique firms delivering to enterprise business. Role: Quality Engineer Medical Devices Location: San Diego, CA Responsibilities:

  • Quality Engineering is responsible for product and service quality evaluation and control. Works cross-functionally in the development and or maintenance of products or services.
  • The Engineer is involved in resolving the CAPA, Device History Record issues, Labeling, Continuous Process Improvement Process and process-related production issues, activities including equipment, process, materials, and method validation as well as statistical analysis and metrics to analyze those systems and processes being measured.
  • Demonstrates intermediate knowledge of quality engineering policies, principles and best practices.
  • Demonstrates intermediate knowledge of FDA/ISO requirements.
  • Applies statistical sample size calculations to work for quality determination on projects of intermediate scope/complexity.
  • May act as mentor to less experienced team members.
  • Applies intermediate understanding of regulatory requirements (cGMP, FDA, ISO, etc.) to support work with little or no supervision.
  • Writes test protocol, tests, investigations, nonconformance reports, collects data, and writes reports to validate against plan to ensure product is used as intended.
  • Has in-depth experience, knowledge and skills in own job family Applies knowledge and skills to a wide range of standard and non-standard situations.
  • Works independently with minimal guidance Usually determines own work priorities Acts as a resource for colleagues with less experience.
Thanks and Regards Vineet Tripathi Recruitment Manager Stellar Consulting Solutions, LLC. http://www.stellarconsulting.com Phone: 678-935-7282 E-Mail: vineet@stellarconsulting.com LinkedIn: www.linkedin.com/in/vineet-tripathi

Vacancy expired!

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