Regulatory Affairs Specialist

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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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Regulatory Affairs Specialist

  • Specialty:

    Engineering
  • Title:

    Regulatory Affairs Specialist
    • City:

      Roseville
    • State:

      MN
    • Zip Code:

      55113
  • Start date:

    07-12-2019
  • Status:

    Closed
  • Assignment Type:

    Contract
  • Job Id:

    49999

Description

The DAVIS Companies is supporting a global organization that designs and manufacturers products that help individuals with disabilities to lead a better and more fulfilling life. We are seeking a Regulatory Affairs Specialist to help them become complaint through the MDD to MDR transition as most of the product line is sold in Europe. 

An ideal candidate will have the following experience: 

• Familiarity with Europe Medical Device Regulation (MDR 2017/745)
• Experience reading and interpreting regulatory requirements
• Experience documenting product for regulatory compliance
• Experience with Arena product documentation software
• Experience with Microsoft Excel and Word

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