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  • Posted: Jul 14, 2020
    Deadline: Not specified
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    Since opening in 2013, USPGhana has trained more than 1000 professionals from 42 African countries on a range of pharmaceutical regulatory, quality assurance, and quality control functions. USPGhana works with partners to develop skills to deliver quality assured medicines to people who need them most.


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    Medicines Registration And Dossier Compilation Trainer

    USP Ghana provides training courses featuring lectures from working professionals in key sectors.  We are currently recruiting experts to teach Medicines Registration and Dossier Compilation as well as Clinical trails and bio-equivalence studies data evaluation .

    Successful candidate will be responsible for providing training materials and their delivery in the following topics:

    • Active Pharmaceutical Ingredients data assessment in Common Technical Document (CTD): General Information and Properties/Specifications/Stability data assessment.
    • Pharmaceutical Product Development.
    • Finished Pharmaceutical Product data assessment: Manufacturing/ Specifications/Stability Data assessment.
    • Process Validation.
    • Analytical Method Validation.
    • Clinical Trials.
    • Bioanalytical Method Validation.
    • Vaccines.
    • Sterile products manufacturing.

    Required Skills or Experience

    • Applicant should demostrate ability and skills to teach above identified topics.
    • Particular consideration will be given to current national regulators, pharmaceutical manufacturers, and international supply chain consultants

    Method of Application

    Interested persons should

    • E-mail  resume and daily rate/ compensation requirement to   [email protected]
    • NOTE: All trainers are thoroughly vetted to avoid conflicts of interest and ensure compliance with USP’s Code of Ethics, as well as applicable laws and regulations. We also work closely with a potential trainer’s current employer to ensure conformance with applicable internal policies and procedures.

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