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  • Posted: Oct 18, 2024
    Deadline: Not specified
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  • Aspen has a proud heritage dating back more than 160 years and is committed to sustaining life and promoting healthcare through increasing access to its high quality affordable medicines and products. Aspen has a market capitalisation of approximately US$10 billion, is the largest pharmaceutical company listed on the JSE Limited (share code: APN) and rank...
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    Regulatory Affairs Scientist (Epping)

    Description

    • Fine Chemicals requires the services of a highly competent Regulatory Affairs Scientist for the Regulatory Affairs Department.  To qualify for this position the most suitable candidate must fulfil the following requirements.

    Requirements

    JOB REQUIREMENTS:

    • Degree in Chemistry/Pharmaceutical Sciences or equivalent qualification.
    • Good knowledge of chemistry (Analytical and Organic).  Knowledge of local and international pharmaceutical regulations and guidelines would be highly advantageous.
    • Excellent written and verbal communication skills and the ability to interact well with internal and external customers.
    • Minimum of 3 years’ experience in pharmaceutical, cGMP, or chemical manufacturing environment.
    • Proven technical documentation compilation skills, with the ability to critically evaluate and interpret data.
    • MS Office computer literacy, particularly the following applications: Word, Excel, Outlook, Teams, Access and PowerPoint.  Minitab and/or EXTEDO proficiency would be advantageous.

    JOB FUNCTIONS (Brief Summary)

    • Compilation and update of documents to be submitted to Regulatory Authorities.  This includes the compilation of Common Technical Documents (CTDs) in accordance with relevant guidelines and regional requirements.
    • Compilation, update and/or amendment of internal documentation relating to the testing and manufacture of Active Pharmaceutical Ingredients (APIs).
    • Responding to customer (both internal and external) and regulatory authority queries.
    • Ensuring that annual product quality reviews are compiled according to cGMP standards and adverse trends and potential process improvements identified.
    • Implementing changes according to established company procedures relating to the testing and manufacturing process.
    • Compilation and/or update of manufacturing and cleaning instructions according to internal procedures and in line with regulatory expectations.
    • Compilation of process qualification protocols and reports.
    • Ensuring that related databases are updated to allow for the capturing of API data.

    PERSONAL ATTRIBUTES (Brief Summary)

    • Good interpersonal skills.
    • Good organisational and systems implementation skills.
    • Exceptional attention to detail and accuracy.
    • Good communication (written and verbal) with excellent report writing and document reviewing skills, including the ability to evaluate data critically.
    • Ability to perform tasks concurrently.

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to Aspen Pharma Group on aspen.mcidirecthire.com to apply

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