QAV Engineer - Life Science - 12-Month Contract
Our client, a global pharmaceutical company, is seeking a QAV Engineer to join their team at a state-of-the-art pharmaceutical facility.
Responsibilities:
* Coordinate and participate in the validation and quality assurance of site equipment, utilities, processes, and software in compliance with policies, FDA, European cGMP, and GAMP standards.
* Develop, maintain, and execute the Site Validation Master Plan.
* Generate, maintain, and execute Project Validation Plans and schedules.
* Create validation protocols and final reports to cGMP standards.
Requirements:
* Degree in engineering or scientific discipline.
* 3+ years of validation/quality experience in medical device plastics processing, moulding, or assembly operations.
* Knowledge of cGMP and regulatory requirements relating to the medical device industry.
This role requires a unique blend of technical expertise and project management skills. If you are interested in this opportunity, please review the full job description below for more information on responsibilities and requirements.