Solheim is working with a Pharmaceutical company in North Carolina that’s looking for a Quality Engineer. Great benefits and relocation offered. Below are the duties and responsibilities for the role.
Duties and Responsibilities:
* Review validation documents
* On the manufacturing floor Subject Matter Expert (SME)
* Understanding and experience validating process equipment and analytical methods.
* Certified Quality Engineer is a must
* 5 years working with Computer System Validation (CSV) is a must
* Understanding of regulatory requirements for FDA and EU
