Our client has an analytical method developed for a substance that is used in the manufacture of an over the counter, commercial medical device.
Ensuring that any confidential information or personal data related toProPharma Group and its clients is managed in accordance with DataPrivacy regulations as described in ProPharma Group Standard Operating Procedures (SOPs).
This position is critical in ensuring that all information is loaded, updated, and maintained within the validated database for use by the ProPharma Group staff on behalf of its clients.
The on-site time at the company would be for help to implement Master Control (others will take the lead), set up the QA unit, and preparing for a potential FDA inspection after the NDA is submitted.
This position is primarily responsible for answering medical inquiries from health care professionals and patients using the available medical information resources at ProPharma Group.
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