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Requirements:
BA/BSc. Degree in Mechanical / Biomedical or equivalent practical experience.
1-2 Years of proven Verification Process Validation experience in medical device industry with a strong emphasis on problem solving, along with written and verbal skills.
Knowledge and experience with Medical Device Quality Systems, ISO 13485, FDA.
Knowledge and experience with environment, safety, bio-compatibility, sterility and essential performance tests (IEC 60601, EN 61508, ISO 10993-5, ISO 11135, etc.).
Solidworks, ERP /PDM
Good documentation skills and ability to communicate effectively at all levels of the organization.
Multi-tasker, independent, punctual and accurate with excellent organizational skills, Team oriented, collaborative, good personal relationships.
Excellent skills in English language are required (verbal and written communication).