Responsibilities:

• Maintain and update technical files for compliance with current regulatory standards.
• Maintain and update the clinical evaluation documentation
• Training and advising personnel in to ensure European requirements.
• Working with engineering and technical personnel to ensure continued compliance to any revised referenced standards.
• Participating in the development and review of quality system

Qualifications:

• BS Degree is preferred
• Must have experience working in Regulatory Affairs within the medical device industry.
• Must have experience maintaining and updating European technical files
• RAC Certification is a plus.
• Must be able to meet deadlines and be detail oriented.
• Good planning and organization skills are a must.
• Must have a strong knowledge of MDD requirements
 

Candidates must live local and be a US Citizen or Green Card Holder

Email resume to: jobs@cwsciences.com

Commonwealth Sciences is a professional recruiting firm specializing in science, engineering and green technologies. We unite industry professionals with exciting career opportunities by leveraging our technical expertise, advanced recruiting tools and years of staffing experience. CWS works with a variety of disciplines and levels from Research Associates to Scientists, Engineers, Managers and Directors. Our clients value the basic integrity, customer service and industry expertise that defines our organization.

Commonwealth Sciences, Inc.
www.cwsciences.com