Vacancy expired!
- Support MDR remediation work on assigned Design History Files including but not limited to: a gap assessment to appropriate industry standards and internal procedures, generate rationales, and perform design and development activities.
- Prepare full DHF documentation in accordance with relevant internal SOPs and Design Control.
- Effectively communicate and work cooperatively with others as part of a team.
- Share information, status, needs, and issues with the site lead and project team members in order to inform, gain input, and support decision-making.
- BS in science or engineering or equivalent experience.
- 0-3 or more years of Engineering related experience; Medical device experience preferred.
- Experience with regulated documentation, design control, and remediation activities highly desired
Vacancy expired!