Requires a Bachelors degree in Health, Life Sciences, Engineering or related field and 5 years of experience in medical device quality, regulatory, clinical or engineering discipline or related position. Must have 5 years of experience in a medical device clinical strategic andor management role; must have 5 years of experience with overall riskmanagement process as it relates to total project lifecycle; must have 5 years of experience with global regulations for product surveillance, risk management and clinical evidence e.g. EU Medical Device Regulation; must have 5 years of experience of Medical Writing Experience relative to CERs; must have 2 years of project management experience; and must have 1 year of people management experience. Telecommuting work arrangement permitted position may work in various unanticipated locations throughout the U.S.br br Requires a Masters degree in health, life sciences, engineering or related field and 3 years of experience in medical device quality, regulatory, clinical or engineering discipline or related position. Must have 3 years of experience in a medical device clinical strategic andor management role; must have 3 years of experience with overall riskmanagement process as it relates to total project lifecycle; must have 3 years of experience with global regulations for product surveillance, risk management and clinical evidence e.g. EU Medical Device Regulation; must have 3 years of experience of Medical Writing Experience relative to CERs; must have 2 years of project management experience; and must have 1 year of people management experience. Telecommuting work arrangement permitted position may work in various unanticipated locations throughout the U.S.
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