US-NJ-Warren: Quality Assurance Director Specialist

To see other opportunities, please visit http://sqa.fyicenter.com
Date: 24-Oct-2008

Quality Assurance Director Specialist

Requirements In this role you will be responsible for oversight of all QA/QMS functions throughout the company currently impacting RUO product operations as well as regulated IVD product design and development, clinical material production, and operations compliance. The Director also oversees QA operations which include: Release (PCR/assay, instrument and software) and PCR/assay stability testing of diagnostic and RUO products, management of a CLIA compliant lab supporting product development, Protocol development and management of testing and validations for new products and development, Assists in the support of regulatory submissions (ie: assay, instrument and software validations), and Training and management in QMS support areas including environmental monitoring and controls. Budgetary and administrative responsibility for all QA staff. Required is a BS or BA degree in Science or Engineering with a minimum of eight years experience in increasing QMS responsibility. This position requires someone with excellent organization, teambuilding, time management and communication skills, QMS management representative experience and software QA management experience.

For more information, please write to us.

Thank you,
Team SQAFYI - Software QA Resource FYI
http://sqa.fyicenter.com