QA associate

• •   Advance knowledge and work experience with Medical Device Quality Systems, ISO 13485:2003 and CFR21 Part 820 • •   Experience in establishment and maintenance of statistical techniques and sampling plans for QC and/or in-coming inspections • •   Advance experience in QC techniques for electrical equipment manufacturing • •  Above 3 years of relevant experience in medical device industry (IVDD electrical equipment) • •   Experience with CAPA, MRB and customer complaints treatment processes •   Ability to write reports and procedure manuals required; • • Strong interpersonal, verbal and written communication skills • •   Time management skills with the ability to multi-task are essential. • •   Proficiency in MS Office Minimum Requirements A degree in engineering, science, bio-science ,  biotech or related background . • •   3+ year's experience in medical device industry required •   Self-motivated and highly organized המשרות באתר פונות לנשים וגברים, כאחד.