Regulatory Assistance for Ruth Sharples

The current project with this business is now at the point where a quality management system needs to be set up and maintained in accordance to ISO 13485. Because of this they are looking for an RA/QA associate to help assist the RA Specialist. General Responsibilities; - Drawing strategy for implementing Quality management system. - Setting up and maintaining all aspects of QMS. - Maintaining and monitoring technical file documentation. - Assisting RA specialist with all Regulatory procedures. - Leasing and brain storming through issues that may arise throughout the project. The company is looking for somebody with 2-4 years experience within a Quality or Regulatory background within medical devices. Also required is the ability to make decisions on own and influence the team's decisions. Required Experience; - Proven working experience of setting up and working with Quality Management Systems. - Strong knowledge of Regulatory Requirements. - 2-4 years experience within medical devices. - Ability to work independently and within a team. To find out more, or inquire about any other roles please call Joseph on 02077587322.

To find out more about Real please visit www.realstaffing.com [1]

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[1] http://www.realstaffing.com/uk