Regulatory Manager/Head

Lobo Management

We are looking to hire a Regulatory Manager/Head for our client which is a leading business conglomerate with diversified business across middles east, India and Africa in different verticals including retail, FMCG, Manufacturing, hospitality, Construction, and healthcare.

For their healthcare/Pharmaceutical division they are looking to hire a Regulatory Manager/Head who will be the senior most person in the Regulatory department and will have the responsibility to manage the department from the scratch which gives the opportunity to a person to grow with the Organisation. We need someone who can work from the scratch initially and gradually develop the department in the coming years. 
Following are the job requirements: 

  • The primary responsibility includes new products submissions, minor variations, post approval reporting obligations and general product life cycle management applicable to UAE and regional countries.
  • 4+ years of solid Regulatory affairs experience in UAE & GCC countries in a medium to large size reputable organization/s for pharmaceutical products.
  • In-depth understanding of regulation in UAE & GCC countries for registration of Innovator pharma product/ Generics pharma products / Herbal products GSL & nutraceuticals / Medical devices / DM approvals for food /cosmetics etc.
  • New Product registration, New Manufacturing Site/ MAH registration & relevant CPP/FSC legalizations experience. Preparation of regulatory dossiers & knowledge of eCTD software’s, eCTD dossier compilations. (Must have submitted a minimum of 2-3 submissions in last 1 year).
  • Re-Registration / Minor variations / appeal of price revision of the product.
  • For assigned products, Patient Package Inserts, local physicians’ circulars, packaging material, Artwork, labelling approvals, analytical calculations experience.
  • Knowledge of analytical labs requirements for herbal and GSL products.
  • Knowledge of preparation of all modules in regulatory dossier including bioequivalence / stability / ICH guidelines etc.
  • Knowledge of DCC, HAAD Code & market access documentation.
  • Prepare and update week, monthly project plans, timelines of approvals and planned submissions to management.

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