Upgrade Post project

QA Specialist/Scientist

Pleasanton  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Keywords

Description

  • Serve as Quality Partner for local QARs, EQNCs, CAPAs and Trackwise entry assuring completion in a timely and compliant manner
  • Review and approval of Clinical Validation Plans, Clinical Protocols and Clinical Reports
  • Review and approval of local IQOQ protocols
  • Review and approval of Design History Files including Design Protocols, Reports and Plans
  • Provide assistance during audits of the Quality System and Clinical Operations

    • Qualifications:

    Bachelor's degree in Biological Sciences or related field, or equivalent combination of education and work-related experience.

    >3 years experience in medical device, pharmaceutical, biochemical industry

    Effective communicator, self motivator, demonstrated ability to work in team envirnonment and build strong internal relationships, quick learner
    Start date
    08/2014
    From
    Real Staffing
    Published at
    26.07.2014
    Project ID:
    748465
    Contract type
    Freelance
    To apply to this project you must log in.
    Register