Description
A leading medical device company in the Long Beach area is looking for someone to fill a position as a Quality Assurance Supervisor who would oversee a small team workign on their newest product.Experience:
* 6 years of experience in Medical Device field
* Knowledge of cGMP/GLP Regulatory requirements
* 5+ years of experience in a lab
Essential Duties and Responsibilities:
* Manage the review, approval and disposition of Raw Materials
* Review and approve data generated for product release, method validation, product stability protocols and reference standard qualification.
* Review and approve deviations, laboratory investigations, out-of-specifications and corrective actions related to data review to ensure compliance and completion within a specified time frame
* Provide resolution, tracking and trending of laboratory investigations, out-of-specifications, deviations and corrective actions related to data review.
* Review and approve method validation reports.
If you or someone you know fits this role please contact me ASAP so we can get an interview set up next week.
To find out more about Real please visit www.realstaffing.com