Health, LLC and its affiliates are equal opportunity employers committed to building a diverse and inclusive workforce..., please contact us at . #CH1K About: Confluent Health, LLC and its affiliates are equal opportunity employers committed...
employee referral program, and 401(K) with a 4% employer match. Confluent Health, LLC and its affiliates are equal... About: Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse and inclusive workforce...
employee referral program, and 401(K) with a 4% employer match. Confluent Health, LLC and its affiliates are equal... About: Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse and inclusive workforce...
match. Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse... an accommodation due to a disability, please contact us at . #CH1K About: Confluent Health, LLC and its affiliates are equal...
match. Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse... an accommodation due to a disability, please contact us at . #CH1K About: Confluent Health, LLC and its affiliates are equal...
match. Confluent Health, LLC and its affiliates are equal opportunity employers committed to building a diverse... an accommodation due to a disability, please contact us at . #CH1K About: Confluent Health, LLC and its affiliates are equal...
documentation for pre-market submissions (i.e. FDA 510(k) submissions, Health Canada Device License Applications). This role...
The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies. Responsible for managing and preparing 5...
between InnovativeHealth, the FDA and other international regulatory bodies;Reviews complaints/adverse events for submission of MDRs...
The Quality Engineer will ensure compliance to required standards including FDA and ISO during process development and the manufacturing of medical device components. In addition, this person will have responsibility for identifying and dri...