Medical Product Registration Expert

4 days ago


Jeddah, Makkah Province, Saudi Arabia Jamjoom Pharma Full time

Jamjoom Pharma offers a challenging and rewarding career opportunity for a Regulatory Affairs Specialist. The successful candidate will be responsible for preparing dossiers for submission, collaborating with internal/external stakeholders, and maintaining project status.

Key Responsibilities
  • Collecting and evaluating scientific data for dossier preparation and submission.
  • Developing clear arguments and explanations for new product registration.
  • Preparing renewal and variation files by collecting, collating, and evaluating scientific data.
  • Collaborating with internal/external stakeholders to ensure availability of required documents/samples.
  • Maintaining project status through implemented system(s)/software(s).
  • Utilizing specialist computer software(s) and resources.
  • Evaluating Change Requests and full products' life cycle management.
  • Uploading product information on relevant portals.
Requirements
  • Bachelor of Pharmacy/Science or Master of Pharmacy/Science degree.
  • 1-3 years' experience in regulatory affairs.
  • Regulatory and scientific knowledge for product registration.
  • Excellent oral and written communication skills.
  • Strong interpersonal and collaboration skills.
  • Proficiency in MS Office Applications and eCTD.


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