QA Specialist I in Larkfield-Wikiup, CA at Volt

Date Posted: 2/16/2021

Job Snapshot

  • Employee Type:
    Contingent
  • Job Type:
  • Duration:
    48 weeks
  • Date Posted:
    2/16/2021
  • Job ID:
    268419
  • Contact Name
    Volt Branch

Job Description

Our client is a bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. If this sounds like a company you would like to be a part of then continue reading below:

We are looking for candidates with proven abilities in quality documentation, control, and audits.  Medical device field is preferred with 2-5 years of experience. Coming with expert skills in MS Office and other reporting systems.

RESPONSIBILITIES:

•       Work with groups within the organization to get corrections and clarifications to Quality Documents finalized.

•       Support Document Control activities including document review and change orders, as required. 

•       Collect and analyze quality metrics and supply these for Management Review Meetings.

•       Collect metrics for QIP meetings and develop graphics of quality trends for management meetings.

•       Prepare training support materials for the site.

•       Work with Laboratory Operations Trainer to align training resources across the laboratory site.

•       Assist with internal audits and agency audits.

•       Demonstrate commitment to the development, implementation and effectiveness of Quality Management System per ISO and other regulatory standards.

PREFERRED QUALIFICATIONS:

•       2-5 years’ experience in Quality Assurance/auditing; Bachelor’s Degree or AS Degree is a plus, but not required

•       Demonstrated ability to carry out assignments in a timely, accurate manner and accomplishing tasks as required with little or no supervision

•       Ability to interact effectively with all levels of the organization and perform multiple tasks in a fast-paced environment

•       Working knowledge of Quality Assurance in a medical device manufacturing environment, preferably in-vitro diagnostic.

•       Knowledge of Quality System Regulations

•       Strong skills in reporting MS Office

VOLT is equal opportunity employer!