Saudi Arabia Job Openings

Medochemie

SCIENTIFIC OFFICE MANAGER-SAUDI ARABIA

November 4, 2024


Medochemie Ltd is an International Pharmaceutical Company headquartered in Cyprus. Medochemie manufactures a wide range of products divided into more than 10 therapeutic categories, owns 4355 marketing authorizations and operates in more than 107 countries around the world. Our thirteen separate manufacturing sites are designed to fully comply with European and WHO current Good Manufacturing Practice (c GMP).
We ‘re on a mission to find the best talent out there. We are now looking for a talented Scientific Office Manager to join our team in our offices in Saudi Arabia.

Duties:

    • Ensure company commitment with local regulations and maintain ethical standards in its scientific and medical activities.
    • Implement regulations and instructions issued by local authorities.
    • Verify marketing information (eg drug indications, safety profiles & dosage instructions) aligns with the approved labelling and promotional guidelines authorized data by regulatory authorities.
    • Provide accurate drug information to beneficiaries (patients) and health healthcare providers, pharmacists, and caregivers.
    • Promote health awareness and drug education.
    • Support and participate in scientific activities and education programs.
    • To contribute to scientific research with specialized centers (as centers carry the bio equivalence studies) when needed.
    • Follow up with the Regulatory Affairs (RA) department on the registration of pharmaceutical preparations thorough SFDA and GHC to ensure all required documentation and submissions for registering new pharmaceutical products or renewing existing registrations are completed on time.
    • Act as the official representative of Medochemie LTD in dealings with regulatory authorities (SFDA and GHC).
    • To organize meetings with SFDA/ GHC to clarify any issues related to new registrations/ renewals/ variations in well-structured, and on timely manner. To work very closely with SFDA/ GHC authority as per direction/ input shared by HQ/Management on various projects.
    • Provide and properly store free samples of registered drugs, this involves managing the distribution, storage, and tracking of samples to ensure compliance with local regulations.
    • Monitor drug quality, effectiveness, and side effects of the company products and ensure these are communicated to the RA department and regulatory authorities.
    • Follow up updating the PIL and packaging to ensure compliance with approved information in coordination with the RA.
    • follow up the protection of patents and manufacturing rights of company drugs in coordination with the relevant stakeholders,
    • Act as Deputy QPPV in the absence of the local QPPV

Qualifications:
    • Applicant should be Saudi national.
    • Must be a licensed pharmacist by the Saudi Council of Health Specialties.
    • A minimum of two years of experience in the same position is required.


We are offering an attractive remuneration package and a challenging opportunity for professional development.

If you wish to work in a pleasant, modern, professional environment with excellent career opportunities, please click buttons below.
Applicants should note that based on the General Data Protection Regulation (GDPR), all applications/CV’s kept in our database have been deleted. In case you have forwarded us your CV in the past and you are interested in this position, please apply again.

All applications will be treated in strict confidence.



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