Job Summary

A leading medical technology company is in need of a Remote Regulatory Affairs Specialist in Sacramento.

Individual must be able to fulfill the following responsibilities:

• Conducting labeling, marketing, product transfer and literature review
• Establishing and maintaining regulatory information systems
• Authoring submissions and other regulatory documents

Required Skills:

• Bachelor’s Degree (B.S or B.A) required
• Previous experience with Medical Devices, Regulatory Affairs, Quality or Engineering
• One year of experience in an FDA regulated industry
• Excellent interpersonal, written English and oral communication skills
• Proficient in Microsoft Office Suite, including Word, Excel and PowerPoint