QAV Engineer - Life Science - 12-Month Contract
Our global pharmaceutical client is seeking a QAV Engineer to join their state-of-the-art facility.
Responsibilities:
* Coordination and validation of site equipment, utilities, processes, and software in compliance with policies, FDA, European cGMP, and GAMP standards.
* Development and maintenance of the Site Validation Master Plan.
* Creation of Project Validation Plans and schedules.
* Generation of validation protocols and final reports to cGMP standards.
Requirements:
* Degree in engineering or scientific discipline.
* 3+ years of validation/quality experience in medical device manufacturing.
* Knowledge of cGMP and regulatory requirements for the medical device industry.