Manager - Regulatory Affairs (south Africa)

India Pharma People
  • Mumbai
  • Confidential
  • 6-10 years
  • 227 Views
  • 12 Aug 2015
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  • Compliance/ Regulatory

  • Pharmaceuticals/ Life Sciences/ Clinical Research
Job Description

Review, prepare & compile CTD/ Dossiers for various dosage forms (tablets / capsules / granules / liquids) for submission to South African regulatory authorities.
Provide timely response to comments/ queries received from regulatory authorities.
From a reputed pharmaceutical company manufacturing dosage forms.
Well versed with preparation of dossiers & other documents for registration in SA.

Desired candidate profile:-

Edu : M.Pharma

Yrs of exp :6-10 yrs

Exp details : Should have experience in handling Regulatory Affairs for South Africa market for formulation.



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India Pharma People