القائمة الرئيسية

الصفحات

Regulatory Affairs Project Coordinator At Novo Nordisk

 Regulatory Affairs Project Coordinator At Novo Nordisk

Regulatory Affairs Project Coordinator At Novo Nordisk

Tasks:

Your other tasks will include supporting the affiliates in ensuring timely compilation and submission of product supply related registrations to maintain timely supply of products to the markets and support your direct manager in other tasks to ensure appropriate governance in relation to Regulatory Operations.

*Up to one week every month is required to be spent in the BAMEAC regional office in Istanbul, Turkey.

Qualifications

To qualify for the position you must have:

A university degree, preferably related to pharmacy, life science or pharmaceutical studies
MSc (Pharm) is desired
Minimum 1-3 years’ experience in Regulatory Affairs as an RA Associate, RA specialist, or labelling coordinator
Fluency in Arabic and English (both spoken and written)

Apply Here

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