Description
Are you a professional with a minimum of 3 years experience in development of medical devices?POSITION REQUIREMENTS:
* Science degree (BSc or MSc)
* Several years experience in quality assurance
* Several years experience in the medical device industry
* Very good knowledge of the regulations related to medical devices
* Good experience in writing and reviewing of design control documents as well as in the compilation of design history files
* Strong communication and organization skills
MAJOR RESPONSIBILITIES:
* Responsibility for activities related to quality and design control
* Responsibility for activities regarding process development
* Management of design control and quality as well as regulatory guidance projects
* Support of process improvement and GMP activities
* Management of the documentation related to design control
* Support of compliance projects
* Responsibility for QA agreements
* Development and management of CAPA's
To find out more about Real please visit www.realstaffing.com