Usa-regulatory affairs specialist ii (clinical) - united states, cambridge bay
support the device regulatory lead in eu medical device regulation (mdr) article 117 related activities and change control assessments for combination products. provide assistance with filing preparations related to eu notified body opinions. perform maintenance activities related to change control assessments for combination products. support the the development of ways of working (wow) guides for the global regulatory affairs device role.
years of experience: 3 - 6 years. experience with combination products, medical device regulations, global device regulations is a plus.
equal opportunity employer/veterans/disabled
the company will consider qualified applicants with arrest and conviction records
--
United States, Cambridge Bay ,Massachusetts
2022-07-13
2022-08-12
1728743
Please report inappropriate ads by sending a message to abuse@expatriatesjobs.com. Please include the Job ID located in the header of each ad
Apply to this job now Report abuse