QA Technician - Validation

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  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
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QA Technician - Validation

  • Specialty:

    Manufacturing
  • Title:

    QA Technician - Validation
    • City:

      Chaska
    • State:

      MN
    • Zip Code:

      55318
  • Start date:

    07-21-2020
  • Status:

    Closed
  • Assignment Type:

    Contract To Hire
  • Job Id:

    54135

Description

DAVIS Companies has partnered with a leading Biomedical Manufacturing company to identify a QA Validation Technician. LOCAL candidates only please. 

The QA Validation Technician will assist in the sustaining of a robust Master Validation Plan and support the MVP strategies. You will be a member of a team responsible for Validating equipment, processes, test methods, and non-product software.

Responsibilities of the QA Validation Technician:

  • Developing test cases and Validation documentation.
  • Execution of Validation Protocols.
  • Support Validation Review Board charter and continuous improvement efforts.
  • Adherence to defined corporate and local validation practices and procedures.

Requirements of the QA Validation Technician:

  • AAS degree & 3 years of relevant experience OR BS in Engineering, Biomedical Engineering, Life Sciences or other relevant degree & 1-2 years of relevant experience
  • ASQ CQE and experience in the Medical Device industry strongly preferred
  • Experience in software, test method, equipment, process and/or design testing methodologies.
  • Ability to evaluate specifications and requirements for completeness and testability
  • Generate test cases and procedures from specifications with minimal guidance
  • Execute test procedures with minimal guidance
  • Experience in testing of systems related to Medical Device 
  • Experience with 21 CFR 820 or ISO 13485 Process Validations

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