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Regulatory Affairs Specialist

Glaxsan Pharma
New Cairo, Cairo
Posted 4 years ago
81Applicants for1 open position
  • 18Viewed
  • 1In Consideration
  • 4Not Selected
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Job Details

Experience Needed:
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Job Description

About the Job

1- Responsibilities:·

  • Preparation of the regulatory documents required for submission of the annual/complementary Importation Licenses and or importation approvals of FRANCO Products and working closely with the DRA / GRA team to ensure that the documents are valid and complete at the time of submission (CPPs, registration licenses, pricing certificates, variations approvals, etc.) ·
  • Working with different internal stakeholders in order to receive the documents required for issuing special import licenses for non-registered products (SILs) on a timely manner.

2- Submission

  • Filling in all MOH forms and templates required for submission.
  • Submission of the importation plans/approvals together with all the related documents to the concerned departments at MOH (Registration department – licensing department – importation department).
  • Submission of SILs requests to MOH.
  • Following up and answering MOH queries in timely manner until granting the final approvals and sharing them with all concerned stakeholders

3- Inspection & Release Follow

  • Follow up on the inspection and release visit.
  • Follow up on the release tracker and sample conformity reports tracker.
  • Working closely with the supply chain and Department of regulatory Affairs (DRA) release colleagues and providing support to ensure final release/inspection of the upcoming shipments are done on a timely manner.
  • Follow up on Health Authority communication in terms of Drug shortage as well as inspection visits schedule.
  • Follow up on the reference standards tracker tool.

4- Others

  • Perform other duties as assigned.

Job Requirements

Skills:

  • Bachelor of Pharmaceutical Sciences or Science Degree.
  • Minimum 2 years of experience within the pharmaceutical industry Experience in regulatory/ importation processes and/or inspection & release of medicinal products.
  • Experience in different types of interaction with regulatory authorities Good planning and organizational skills and ability to manage a large workload under pressure and to cope with tight deadlines.
  • Ability to foresee and respond to potential problems and opportunities.
  • Negotiation & Communication Skills.
  • Leadership skills.
  • Strong interpersonal skills.
  • Good Command of English Language.
  • Computer Skills.
  • Full Time.

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