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  • Posted: Jun 6, 2017
    Deadline: Not specified
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    Wildlife Pharmaceuticals is a small manufacturing company, based in White River, South Africa, which specialises in niche, small batch, and regulated medicines. Established in 1997, and borne from a passion to research, develop, manufacture and register products dedicated to the wildlife veterinarian, we conquered to deliver to this sector, tested products o...
    Read more about this company

     

    Responsible Pharmacist

    Job description

    We are looking for a responsible and honest individual to be part of a dynamic work environment with pharmaceutical diversity.

    If you are enthusiastic about pharmaceutical regulations and the process of registering a new medicine, give us a chance to meet you.

    We expect you to have extensive knowledge about the path of medicine registrations and pharmaceutical import or exports. We want to see a committed and approachable

    individual and be impressed with your character and skills.

    The goal will be to register medicines for veterinary and human use in accordance with the guidelines from a Good Manufacturing Practice perspective.

    Responsibilities

    • Responsible for continuous supervision of the pharmacy of which he/she has been appointed
    • Ensure there is compliance with Good Pharmacy Practice as published by the Pharmacy Council
    • Establish policies and procedures for the employees of the pharmacy with regard to the acts performed and
    • services provided in the pharmacy
    • Ensure correct and effective record keeping of the purchase, sale, possession, storage, safekeeping and
    • return or distribution of medicines or scheduled substances
    • The ability to handle a medicines recall or withdrawal
    • Handling of product complaints
    • Handling of rejected goods in a procedurally correct manner, the disposal or destruction of medicines
    • To perform self-inspection audits on the contract manufacturing facility
    • Responsible to the Medicines Control Council for compliance with the provisions of the “Medicines and Related Substances Control Act”, Act 101 of 1965
    • Implementation of post-registration amendment guidelines
    • Import and Export of medicines according to referenced guidelines

    Requirements

    • B Pharm Degree
    • Minimum of 5 years regulatory experience
    • Preference towards GMP Manufacturing exposure

    Method of Application

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