Regulatory Affairs Specialist

Regulatory affairs with Technical Files, or equivalent in an R&D or quality position with hands-on experience in the preparation, review, and/or auditing of medical device DHFs, Risk Management files, and/or DMR’s.

Must have knowledge of European/International and US regulations and standards; Experience in preparing and content of technical files and design dossiers; Experience with preparation, review, and/or auditing

To know more about the position or to schedule an interview, please contact:

Sagar.rathore(at) collabera.com

630-485-2166