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Spec 3, Regulatory Affairs (Consult, Reg Affi Mfg. (FDA)) Job DescriptionResponsibilities: Ensure timely execution of regulatory strategies and customer deliverables as determined by RA Manager Manage and execute end to end activities, such as documentations, submissions and addressing health authority questions for new or renewal of existing medical device registrations of Reusable Pen and pen needles in worldwide market Maintenance of compliant regulatory files and supporting documentation (EU technical files/ US master files/international technical. After registering you may be able to apply for this job directly (if still active) on (Katalyst Healthcares & Life Sciences)'s site. Future job matches may be sent from Geebo approved job partners.
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