3 - 9 years’ experience in Regulatory Affairs, preferably in EU procedures and regulations, Variation filing etc. Knowledge or experience in CTRS will be an advantage.
Understanding of global regulatory submission formats, industry standards.
Preparation, compilation and submission of product registration dossier to health authorities for different formulation in CTD, ACTD and eCTD format.
Remote option is available.
CTC- 8-13 LPA
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