The SME will be responsible for bringing the company into compliance with the new ISO 13485:2016 med device guideline. Hands on experience with ISO 13485 is required, and experience with the ISO 13485:2016 guideline and/or certification is a plus. The successful candidate will possess strong gap analysis skills, and will perform a gap assessment between ISO 13485:2003 and ISO 13485:2016 guidelines for the client. Consultant will then make recommendations and drive the process to bring the company into compliance with 2016 guidelines.
Location: NJ | Job Type: Contractor
