Product Registration• Registration of the all the cosmetic products as per guidelines in respective GCC markets.• Collection of all relevant documents (manufacturing/artwork) from Internal and external stakeholders.• Applying for NHM Mark certification on MOAIT website for the hala certified products

1.End to End responsibility of formulation development till the dossier filling stage.2.Update to senior management on the status of the projects3.Risk analysis & timely escalation to management4.Adherence to project management methodologies5.Develop work plan including activities, analysis, deliverables, resources, stakeholder management and communication plan.6.Work with/manage project teams to help deliver projects. Specifically,* Guide teams in setting up and conducting analysis* Ensure project stays on time and key milestones are being met* Ensure stakeholder alignment* Facilitate decision making

•Addressing Queries/Deficiencies related to Formulation & Development. Responding to queries and RFIs received from Regulatory agencies of TGA[Australia], MEDSAFE [New Zealand], EMEA [Europe], Russia, CIS regions, Canada and ASEAN countries. 1.Facilitate in addressing the queries related to tightening of Dissolution, Water content, Related substances, Residual solvents limits by evaluation of the available data. 2.Application of Test licenses, Import license, declarations and required documents to RA. 3.Facilitate in proposing the particle size limits and ranges for the API that are known to exhibit poor solubility according to Bio-pharmaceutical Classification Systems. 4. Generating additional stability data (Photo-stability, In-Use stability, freeze-thaw study) to address the queries. 5.Actively involved in raising of Change Controls & uploading of protocols in SAP database 6.Facilitate in including additional test parameters in the existing specifications when requested by the MoHs of the Regulated markets. 7.Providing the finished product, innovator samples, stability samples & placebos to Analytical dept to address the analytical related queries. 8.Providing the justifications or supporting data on having two excipients with same functions in the manufacturing formula, Not amending the specification limits of the test parameters when requested by the MoHs of the Regulated markets 9.Changing the colorant (coating agent) or Capsule color, of the dosage form when requested by the marketing team or the MoH of the regulated markets during the product registrations.TROUBLING SHOOTING FOR REGISTERED FORMULATIONS/ QIP (QUALITY IMPROVEMENT) PROJECTS Design and facilitate the development of solid & semi-solid oral dosage forms for regulated as well as domestic market within agreed time lines. Plan and execute Innovator Characterization, formulation development, scale up batches and initiation of stability studies according to ICH guidelines.

Generic formulation development