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Registration Officer (Pharmaceuticals)

1.00 to 10.00 Years   Kuwait   07 Apr, 2023
Job LocationKuwait
EducationNot Mentioned
SalaryNot Mentioned
IndustryPharmaceutical Manufacturing
Functional AreaNot Mentioned

Job Description

Policies & Procedures

  • Implement the Pharmaceuticals Division?s policies and procedures and comply with Mohamed Naser Al ? Hajery & Son?s other policies.
Registration Activities
  • Implement all activities related to Regulatory Affairs including ensuring that all Medicines provided by the Pharmaceutical Division are distributed in compliance with appropriate legislation.
  • Complete regulatory submission forms and file the same along with the necessary accompanying documentation while ensuring maximum efficacy and accuracy.
  • File submission renewals (in coordination with the Regulatory Affairs Unit Head) to the MOH or related Regulatory Authority, as deemed necessary.
  • Follow-up with the MOH or related Regulatory Authority regarding the progress of regulatory submissions and inspections, to ensure timely completion of the same.
  • Attend continuing education courses as often as necessary to keep current on changing RA policies and procedures
  • Forward all complaints received from Mohamed Naser Al ? Hajery & Son?s Divisions/ Departments against parties infringing on Mohamed Naser Al ? Hajery & Son?s rights to the Regulatory Affairs ? Unit Head.
  • Implement preventive fraud regulations as per MOH regulations and instructions.
  • Maintain an excellent knowledge of all Medicines provided by the Pharmaceutical Division.
  • Keep up to date with all amendments to the regulatory legislation and guidelines.
  • Ensure compliance with all MOH regulations and other regulatory authority decrees.
  • Ensure Mohamed Naser Al ? Hajery & Son?s terms of use are properly published in all sales outlets, on marketing brochures and on websites.
  • Ensure that all labelling, storage and packing activities related to all medicines are implemented accurately and efficiently in line with the set guidelines.
  • Ensure that all required documents are up-to-date and adhere to the quality standards required by the Regulatory Authorities to avoid any rejection of Medicines.
  • Perform ad-hoc and other duties related to the job as assigned by the Direct Manager.

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