Description
A leader in medical devices and pharmaceuticals, located in northeastern Illinois, is in need of a Quality Consultant to support a large scale remediation effort.The Quality Consultant will have the following responsibilities:
- Remediate risk management files
- Assist in developing Design History Files
- Update risk management files to be compliant with ISO 14971
- Review and approve RMP, FMEA, and RMR documentation
- Work cross functionally
- Act as team lead when appropriate
The Quality Consultant must meet the following requirements
- B.S. Engineering or a related field
- 3-5 years experience in the Medical Device or Pharmaceutical industry
- Experience developing DHF
- Experience in risk management
- Experience working with combination products preferred
- Excellent communicator
- Independent worker
This is a 6 month contract which will expose you to remediation, a very sought after skill within the medical device industry. If interested please apply now!
To find out more about Real please visit www.realstaffing.com