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Regulatory Affairs Supervisor

Amico Group
Cairo, Egypt
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Regulatory Affairs Supervisor

Cairo, EgyptPosted 14 days ago
15People have clicked1 open position

Job Details

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Job Description

Job Purpose:
Responsible for the products registration and renewals, as well as the fulfilment of all regulatory requirements to import, market and utilize AMICO products. 
Key Responsibilities
  • Develop new regulatory policies, processes and Standard Operating Procedures and train key personnel on them.
  • Serve as Central Reference point for all regulatory affairs for both AMICO and its suppliers.
  • Assist as needed in providing necessary documentation or information to support import and export of regulated products, including FDA Importation Codes, and Certificates to Foreign Government for Medical Devices.
  • Monitor and advise impact of changing regulations on submission strategies and update internal stakeholders.
  • Assist in the development of multicountry regulatory strategy and update strategy based upon regulatory changes.
  • Assist in regulatory due diligence for potential and new acquisitions. Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities.
  • Compile, prepare, review and submit regulatory submission to authorities. Report adverse events to regulatory agencies and internal stakeholders.
  • Represent AMICO to authorities whenever required.
  • Provide strategic input and technical guidance on regulatory requirements to development teams.
Qualifications - Minimum Requirements:
  • Bachelor’s degree or equivalent
  • Professional Certificates: RAC
  • Typically 10+ years industry experience in the medical device/pharmaceutical area, with 5+ years supervising Regulatory Affairs in the Gulf countries including KSA.
  • Competencies / Skills: Strong knowledge of gulf / middle east countries regulations.
  • Additional or Desirable Qualifications: Managerial skills, Project Management.

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