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Regulatory affairs Associate Company Name: MaxisIT Assist in preparing and maintaining regulatory submissions (EU, NDA, IND). Prepare responses to questions from regulatory agencies and guidance. Review technical documents for submissions and provide QC checks for accuracy. Participate in cross functional teams for development projects. Maintain regulatory procedures and track and report status. Some knowledge of current FDA regulatory requirements and trends Knowledge of software, EDMS system Ability to work with. After registering you may be able to apply for this job directly (if still active) on ((None))'s site. Future job matches may be sent from Geebo approved job partners.
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