QC control inspector -Lab at SUNDUS MANAGEMENT CONSULTANCY & STUDIES BUREAUL.L.C
Dubai, Dubai, United Arab Emirates -
Full Time


Start Date

Immediate

Expiry Date

18 Nov, 26

Salary

0.0

Posted On

20 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Pharmaceutical Manufacturing

Description

Regulatory Affairs & Warehouse Pharmacist

About Zahrawi GroupZahrawi Group is a leading company in the GCC Healthcare Industry with its presence in UAE, KSA, Qatar, Bahrain, & Oman markets. The company supplies and distributes high-quality products and services to Hospitals, Clinics, Laboratories, & Analytical Industries.

job BriefResponsible for all Product Classification/Manufacturing Site Registration and Product Registration and to ensure that all documents required are available and are submitted on time. They are also responsible for the preparation of the pre- and final perm

Policies & Procedures:

  • Adhere to all Zahrawi Policies & Procedures as applicable.

Regulatory Affairs:

  • Ensure that Zahrawi’s products comply with the regulations of the MOH.
  • Keep up to date with the latest changes in regulatory legislation and guidelines.
  • Liaise and negotiate with regulatory authority to ensure a smooth registration process.

Product Classification & Registration:

  • Ensure that all required documents and actions for Product Classification/Manufacturing Site Registration and Product Registration are available.
  • Prepare all required documents to be submitted for Product Classification under MOH.
  • Prepare all required documents to be submitted for Manufacturing Site registration under MOH.

Importation Permits:

  • Prepare and apply for the pre-permit document as per the MOH guidelines and verify the items being imported and the documents required.
  • Communicate with the existing and new suppliers regarding MOH importation rules and policies.
  • Upload on the MOH importation system any new classifications or registration certificates.

Audit:

  • Prepare any documentation needed for internal and external audits.
  • File all documents in the corresponding files to ensure all are available and are correct.
  • Evaluate the suggestions after the audit and implement them when possible.

Pharmacovigilance System:

  • Responsible for Pharmacovigilance related work and assigned as deputy QPPV.
  • Report Adverse Drug Reactions (ADRs) for all products by collating the needed information and incorporating customer’s comments.
  • Conduct monthly PV activities to keep full compliance with the regulations.
  • Prepare and review all SOP’s Pharmacovigilance plans for all Zahrawi Suppliers.

Medical Devices FSN/FSA Vigilance system:

  • Report the received FSN/FSA to the health Authority and keep align with the reporting timelines.
  • Keep tracking for the reported cases and the health Authority requirements to ensure fulfillment.
  • Keep updated with the new regulations related to the local vigilance system and report them to the manager

REQUIREMENTS

  • Education: Bachelors Degree
  • Additional details:
    • Candidates must be based in the UAE and should be willing to move to company visa
    • Candidates must have a valid MOH license
  • Experience: 2 – 4 years of experience.
  • Job Specific Skills: Require a good knowledge in Pharmacist, Regulatory Affairs, Importation Permits

Location: UAE – DubaiJob Type: FULLTIMEJob Posting Date: 18-09-2023Division/Department: Warehouse Operation and Distribution

How To Apply:

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Responsibilities
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