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Premarket Regulatory Affairs Manager Position Location US-CA-Rancho Santa Margarita Applied Medical is a new generation medical device company with a proven business model and commitment to innovation that has fueled our rapid business growth and .....
Regulatory Affairs Specialist – Premarket Position Location US-CA-Rancho Santa Margarita Applied Medical is a new generation medical device company with a proven business model and commitment to innovation that has fueled our rapid business .....
would you like to be part of a dynamic organization who enable Health Care professionals to improve the lives of their patients in Ophthalmology, microsurgery and other medical growth sectors?the senior Regulatory Affairs specialist is responsible .....
job id: 2018-11147career level: experienceddivision: salt lake city, ut/ Vascular access devices - mdsrelocation: nolocation: salt lake city,utah,united statesoverview:bard has now joined bd is a global medical technology company that .....
description:develops global regulatory strategies for electro-mechanical and Software product submissions.  develops and maintains domestic and international submissions.  reviews international and domestic labeling and Marketing .....
Regulatory Affairs specialist, senior (digital Pathology)responsible for activities which lead to and maintain domestic and international regulatory approval to market devices. responsible for assessment of device changes for regulatory .....
at abbott, we're committed to helping people live their best possible life through the power of Health. for more than 125 years, we've brought new products and technologies to the world -- in Nutrition, Diagnostics, Medical Devices and branded .....
job titlesenior Regulatory Affairs Engineer (m/f) job description in this role, you have the opportunity to provide regulatory Leadership for patient monitor product lines and to build and deliver on competitive regulatory strategies. you work .....
responsible for activities which lead to and maintain domestic and international regulatory approval to market devices. responsible for assessment of device changes for regulatory implications.   essential functions: assist in activities .....
the sr.Regulatory Affairs specialist will be responsible for the preparation of regulatory submissions and Documentation required to market new or modified Medical Devices and In Vitro Diagnostic devices in both domestic and international Clinical .....
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