Quality (QA) Expert
B.A. in Mechanical Engineering/ Biotechnology/ Life Sciences 3 years of experience with medical device Quality and Regulatory requirements (ISO13485, GMP) Experience in writing and implementing Quality system comply with ISO13485 Experience working with R&D and Manufacturing departments Familiarity with the Medical Device Directive (MDD) requirements Has participated at least once in a CE quality/regulatory audit High level English Applying: If you find that you are suitable to the job requirements, we would appreciate your sending of your resume directly to: jobs@rs-ness.com Thank you in advance and good luck * Appropriate inquiries will be answered