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