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  • Posted: Aug 17, 2020
    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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    Quality Assurance Pharmacist

    About

    Conduct in-process compliance to quality procedures, standards and specifications for value stream operations, Review and approve quality related activities for value streams, Identify and provide solutions to systematic issues, Review Annual Performance Quality Review (APQR) as well as related administrative tasks.

    Responsibilities

    Planning and Process

    • Provide technical and operational input during drafting of plans and procedures specific to unit.

    Process Compliance

    • Execute day-to-day QA activities for value streams
    • Identify systematic technical and process issues by reviewing CAPA requests and trends
    • Systematic investigation of the root causes of identified problems and risks for corrective action or prevention
    • Develop CAPA plans and change incidents to address process compliance
    • Implement operational changes to SOPs and processes, in compliance with control processes
    • Ensure deviations (planned/ unplanned) and concessions are documented, reviewed, and analysed; and recommend validation activities to be performed
    • Execute change control process by ensuring changes are documented, reviewed and approved

    Annual Performance Quality Review

    • Review APQRs to assess production risks and quality of in-process control programs
    • Review and analyse CAPA plans to assess impact on quality procedures and standards

    Retention Sample Management

    • Store and manage retention samples as per guidelines

    In Process Quality Management

    • Review and approve outcome of in-process internal inspections

    Reporting

    • Monitor the storage of documents on the soft and hard copy filing systems
    • Maintain and update records and systems as required
    • Provide information for reports on weekly/monthly basis, as required by superior
    • Compile standardised reports and consolidate documents

    Requirements

    Grade: 9

    Background/experience

    • Bachelor’s degree (B Pharm) with 4-6 years’ related work experience, or Post Graduate Degree/ Post Graduate Diploma with 2-4 years’ related work experience
    • Pharmaceutical manufacturing experience

    Specific job skills

    • Advanced understanding of the pharmaceutical manufacturing and corrective action programs
    • Pharmaceutical standards and compliance requirements
    • Ability to interpret and implement policies, processes and objectives

    Competencies

    • Information Gathering
    • Interrogating Information
    • Offering Insights
    • Taking Action

    Method of Application

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

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