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  • Posted: Dec 16, 2024
    Deadline: Dec 20, 2024
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  • Janta Kenya is a HR Consultancy firm established with an objective of encompassing integral and necessary skills that most individuals and organizations need in everyday business. We have a team of professional HR consultants with extensive experience in all people management issues, and we are therefore well placed to offer advice for private, public and n...
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    Quality Assurance Assistant

    Job Description

    Assist in for quality management systems, control and documentation.

    Key Responsibilities

    • Assist in determining training needs, train cGMP and monitoring of compliance with requirements of cGMP.
    • Assist in documentation and evaluation BMRs and BPRs.
    • Assist Reviewing, developing of missing SOPs and implementation of SOPs.
    • Handle product related customer complaints as well as execute and co-ordinate product recalls, together with supporting staff.
    • Convene self-inspections and/or quality audits and make recommendations, where applicable.
    • Assist in ensuring that all requisite validations are carried out.
    • Investigate and set standards for quality and health and safety.
    • Ensuring manufacturing processes comply with standards at both national and international level.
    • Ensuring maintenance of his/her Department, premises and equipment.
      • Carry out vendor audits.
      • Assist in Preparation of training and self-inspection schedules.
      • Specify quality requirements of raw and packaging materials with suppliers.
    • Ensure initial and continual training of Departmental Personnel as necessary.
      • Ensure appropriate manufacturing systems in-process controls are implemented.
    • Review and authorize/reject any document that gives work instructions and set requirements such as procedures, protocols, test methods, and specifications—including changes to these documents.
    • Review and authorize/reject production batch records and make the final decision to release a product lot into commerce.
    • Ensure investigation is conducted and root cause is eliminated for production and control record errors, discrepancies, and failure to meet specification, including quality attributes.
    • Review complaints to determine if it relates to a failure to meet specification, if so investigate and report to regulatory authorities if serious and unexpected.
    • Be independent reviewer and authorizer with respect to manufacturing and process/ product development units.
    • Establish Quality procedures and standards.
    • Authorize written procedures and other documents.
    • Control and archiving of records and documents.
    • Prepare Corrective actions and preventive action (CAPA) records.
    • Retrieval and filling of complete BMRs and BPRs

    Check how your CV aligns with this job

    Method of Application

    Send CV to [email protected] by 20th December 2024.

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