Validation Engineer
Our client, a medical device company in the East Bay area is looking for a Quality/Validation Engineer to join their team.
On a day-to-day basis, this Quality/Validation Engineer will be responsible for:
- working in an FDA environment
- creating and executing validation protocols - IQ/OQ/PQ
- writing SOPs and technical reports
- assisting in creating study/experiment protocols
Qualified candidates must have a BS degree, and 2-3 years of FDA medical device experience, and qualification/validation experience.
Required Skills for Validation Engineer Job:
- FDA
- WRITE SOPS
- IQ/OQ/PQ
- TECHNICAL REPORTS
Join Aerotek CESM, one of the leading providers of engineering and engineering support professionals in North America. Due to our growth, we're constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across a number of different industries. We know it's more than just your day-to-day responsibilities that can make or break a job. It's the support you get. That's the reason Aerotek CE offers a variety of benefits including medical, dental, optical, 401k, and many more. Don't put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek CE team! Allegis Group and its subsidiaries are equal opportunity employers.
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