Regulatory Affairs Specialist

1970-01-01Davis Companieshttp://daviscos.com/wp-content/themes/davis_theme/assets/images/logo.svg325 Donald J. Lynch Boulevard, Suite 201MarlboroughMA01752USAcustomer support[+800-482-9494][+508-481-8519]
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Regulatory Affairs Specialist

  • Specialty:

    Engineering
    • City:

      Roseville
    • State:

      MN
    • 55113
  • Assignment Type:

    Contract
  • Job Id:

    49999
  • Payrate:

    $50.00

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

Quick Apply

  • 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.
  • Accepted file types: pdf, doc, docx, txt, rtf.
  • By applying to this position and providing my contact information, I give The DAVIS Companies permission to provide me with email communications and information.

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