Full Time
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Job Details

  • Responsible for preparation of Registration dossiers of all new products and Re-registered products.
  • Submitting variations of existing products.
  • Responsible for preparation and submission of Analytical dossiers to NODCAR ( National Organization for Drug Control and Research ).
  • Follow up submission and any supporting documents along with registration lead time.
  • Support logistic team with all references, legalized certificates and material needed for regular analysis and release.
  • Prepare analytical files to be submitted to different authorized labs
  • Follow up analysis and supply all needed requirements to get release certificates f samples.
  • Ensures confidentiality in respect of registration files contents.
  • Completing all registration requirements for all shipments at EDA.
  • Responsible for obtaining Ministry of Health importation approvals, inspection & release.

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