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  • Posted: Aug 14, 2025
    Deadline: Not specified
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  • Adcock Ingram is a leading South African pharmaceutical company with a proud 130 year heritage. It has a portfolio of trusted, quality brands and generics and an entrenched value system that assures integrity. Growing from humble beginnings as a small Krugersdorp pharmacy in 1890, Adcock’s portfolio includes an extensive range of Prescription, Over-the-co...
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    Technical Support Team Co-ordinator

    Requirements

    • Matric Certificate.
    • Appropriate tertiary qualification and relevant experience.
    • Pharmacist Assistant Basic / Post-Basic advantageous but not necessary.
    • Computer literacy especially in MS Office mandatory.
    • 3 - 5 years’ experience in a pharmaceutical manufacturing environment.
    • Understanding of GLP, GMP, Regulatory guidelines (SAHPRA, ICH, etc).
    • Knowledge on process validation and related processes highly advantageous.

    Key Job Outputs

    • Evaluate and provide advice with respect to current formulations and processes.
    • Provide improvements for product processes to increase manufacturing efficiencies.
    • Compile protocols and reports for relevant activities.
    • Observe product manufacturing processes in the facility and record data as per approved protocols.
    • Collate, analyse and discuss data in respective reports, and make recommendations.
    • Conduct risk assessments on products and processes.
    • Control and submission of samples for analysis and providing required documentation.
    • Assist with investigations and report writing.
    • Collate data from multiple sources for investigations.
    • Complete investigations with workable solutions.
    • Identify, where possible, root causes of issues and plan a course of action for further investigation and/or corrective actions.
    • Complete investigations within allocated timelines.
    • Evaluate new product manufacturing documentation.
    • Ensure new products are optimised and introduced successfully into the manufacturing facility.
    • Conduct trials as per SOP where necessary using relevant documentation
    • Compile, update and review SOP’s timeously according to current procedures.
    • Raise relevant deviations, change controls, CAPAs and incident forms where necessary.
    • Assist with preventative/corrective actions with regards to audit responses.
    • Ensure all work performed is of the highest quality and in full compliance with GxP’s, SOP’s, regulations and safety standards.
    • Administrative duties (filing and maintaining relevant data bases).

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified? Go to Adcock Ingram on adcock.mcidirecthire.com to apply

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