Description
Responsible for the execution of process development, validation and improvement for a Class III medical device.Requirements:
A BSME degree or higher with at least 5+ years experience in the medical device field.
- IQ/OQ/PQ
- Equipment Validation
- Class III medical device experience
- ISO 13485, ISO 14971
- Implement semi- automation into new and existing processes
- Perform CAD design of complex tooling and equipment
- Risk Management
- PCB experience
Additionally, major pluses are direct experience with infusion pumps or catheters, experience with disposables and consumables and experience trouble-shooting and testing PCB boards.
This is an amazing opportunity for a long term contact or permanent position with a top end client.
Please apply immediately to be considered for an interview.
To find out more about Real please visit www.realstaffing.com