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  • Posted: Jan 8, 2025
    Deadline: Jan 14, 2025
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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...
    Read more about this company

     

    Quality Control Supervisor

    Key Responsibilities

    • Approving or rejecting raw and packaging materials upon delivery.
    • Ensure all necessary Quality Control testing are carried out.
    • Ensure all requisite validations are carried out.
    • Devise and establish company’s Quality procedures, standards and specifications.
    • Sampling of raw materials, packaging materials, bulk products and effluents.
    • Stability studies of finished Goods.
    • Ensure re-testing procedure is followed and customer complaints as well.
    • Monitoring of IPQC.
    • Reviewing, compiling and filling of test reports.
    • Training on cGMP and monitoring of compliance with the requirement of cGMP.
    • Investigating, and taking of samples in order to monitor factors, which may affect product Quality.
    • Document and evaluate Batch Manufacturing records (BMRs)/Batch Packaging Records (BPRs).
    • Approve specifications, sampling instructions, test methods, and other Quality Control procedures.
    • Ensure internal and external calibrations are carried out and records updated.
    • Storage and withdrawal of retention samples.
    • Evaluation of Out of specification.
    • Draft and generate in-house Certificates of analysis.
    • Quality checks and documentation of checklists during receipt of incoming goods from the suppliers.
    • Review and implement Quality Control SOPs.
    • Ensure raw materials and packaging materials have the right status labels.
    • Ensure Good laboratory practices and Good Documentations Practices are implemented.
    • Perform retests or re-examine approved components, drug product containers and closures after long storage or exposure to adverse conditions.
    • Online checklist.
    • Product non-conformity control.
    • Carry out Design and development of new products

    Skills and qualifications;

    • At least 2 years’ experience in a chemical manufacturing environment.
    • Working knowledge of Good Manufacturing Practices (GMP),
    • ISO 9001:2015, SAGE System and KAIZEN is an added advantage.
    • Diploma or Degree in Analytical Chemistry or any related Field.

    Check how your CV aligns with this job

    Method of Application

    If qualified send CV to vacancies@jantakenya.com by 14th January 2025 indicating on the subject line “JOB TITLE”

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