Description
Job Duties:Completes Design History File documentation ,Design of Experiments (DOE) and Statistical Process Control (SPC),Participates in internal supplier audits, Participates in procedure writing and review ,Performs process and equipment validations ,Provides technical support to other engineers ,Reviews product performance data to identify trends, Supports manufacturing, development, and implementation processes, Utilizes FMEA within process development ,Ensures compliance with GMP's, Generates documentation for engineering protocols and reports ,Writes engineering and manufacturing specifications
An ideal candidate has more than 2 years of experience in process validation (IQ/OQ/PQ) in the medical device field.
To find out more about Real please visit www.realstaffing.com