Job Details

  • ID#43833272
  • Address 11747 , Melville,

    New York

    Melville USA
  • Job type

    Permanent

  • Salary USD $75,000 - $95,000 per year 75000 - 95000 per year
  • Hiring Company

    Jobot

  • Showed05th July 2022
  • Date04th July 20222022-07-04T03:00:00-0400
  • Deadline02nd September 2022
  • Category

    Et cetera

Quality Engineer

World leading medical device organization is seeking a skilled Quality Engineer to join their team.This Jobot Job is hosted by: Jeff MatheosAre you a fit? Easy Apply now by clicking the "Apply Now" button and sending us your resume.Salary: $75,000 - $95,000 per year

A bit about us:We are a well-established Medical Device organization that is rapidly growing due to our innovative products. We are looking to add a skilled Quality Engineer who has experience working in FDA AND ISO facilities. If you are a Quality Engineer with 5+ years of experience working in the Medical Device Industry read on!

Why join us?Competitive Pay $75-$95kGreat company cultureStabilityGrowth opportunitiesComprehensive benefits package

Job DetailsEssential Functions and Responsibilities:
  • Review customer complaints, conduct product investigations and ensure proper complaint closure
  • Conduct medical device reporting assessments and investigations.
  • Develop sampling plans for evaluating, and reporting quality and reliability data.
  • Demonstrate continuous effort to improve product quality and manufacturing processes.
  • Participates on Project Team as Quality Representative. Ensures that principles of Design Control are applied to Product and Process Changes and New Product Development.
  • Provides Quality Assurance leadership for Project Teams or Quality departments.
  • Creates reviews and approves Quality System Documents (ex. CAPA, Audits).
  • Creates reviews and approves Product Documents.
  • Creates, reviews, and approves Protocols, Process and Product Validations, Stability Protocols, Software Validation documents.
Work Experience Requirements:
  • Quality Engineering and Customer Complaint Investigation experience
  • Working knowledge of standards and regulations, including but not limited to US-FDA's 21 CFR Part 820 and 21 CFR Part 803, and GMP.
  • Medical Device Industry experience and working knowledge of ISO-13485 and ISO 14971 Medical devices
Interested in hearing more? Easy Apply now by clicking the "Apply Now" button.

Apply This Job

Similar jobs

Quality Engineer

Jobot - Quality Engineer

Quality Engineer

Jobot - Quality Engineer

Quality Engineer

Jobot - Quality Engineer

Quality Engineer

Jobot - Quality Engineer