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  • Posted: Oct 1, 2026
    Deadline: Oct 7, 2026
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    We are continuously upgrading to new technologies and implementing robust processes to ensure we deliver best-in-quality products to our communities

     

    Quality Assurance Manager

    Brief Job Description:

    • Leading, maintaining and continuously improving the Quality Management System (QMS) in line with international cGMP, GDP and GSP standards
    • Acting as a registered Company Pharmacist, fulfilling all legal and regulatory responsibilities of the role, including the release of finished pharmaceutical products to the market
    • Ensuring that all processes, specifications, instructions and results comply with the registered dossiers and with national and international GMP, GSP and GDP regulations
    • Authorizing written procedures and their amendments, including SOPs, cleaning and operating procedures, specifications, analytical methods, validation/qualification and stability protocols, and batch and packaging instructions and records
    • Managing, reviewing and approving the calibration and qualification of equipment, instruments, facilities and utilities, and the validation of manufacturing processes and cleaning procedures
    • Reviewing batch records, packaging records and analytical testing records, and approving or rejecting starting materials, packaging materials, intermediates, bulk and finished products
    • Qualifying, approving and monitoring manufacturers of raw materials, intermediates, packaging materials and finished products, and participating in external audits of vendors and service providers
    • Conducting regular self-inspections and internal audits, managing inspections by authorities and customers, and ensuring timely closure of resulting CAPAs
    • Managing, investigating and closing market complaints and managing product recalls, ensuring timely response to customers and regulatory authorities
    • Ensuring timely preparation, review and approval of Product Quality Review (PQR) reports
    • Preparing, executing, controlling and monitoring the Quality Assurance CAPEX and OPEX budget
    • Acting as the back-up QPPV in the absence of the QPPV
    • Leading and developing the Quality Assurance team
      • Providing functional and disciplinary leadership
      • Ensuring regular and effective cGMP and GDP training of all staff
      • Promoting a strong quality culture across pharmaceutical operations

    Qualifications and Experience:
    Must Have: Minimum Requirements
    To be considered, these minimum requirements must be evident on your resume.

    • Education: Bachelor of Pharmacy degree
    • Registered as a Pharmacist in the Republic of Kenya
    • A minimum of 5 years’ experience in the Pharmaceutical Industry, of which at least 3 years should be in a similar position
    • Expert understanding of local and international regulations and standards for cGMP, GDP and GSP
    • Excellent leadership, reporting and organizational skills, with the ability to design procedures and influence as a team player
    • Self-driven and structured, able to work under minimal supervision, resolve problems in a timely manner and handle high work pressure
    • Proficient computer skills: MS Word, MS Excel and MS PowerPoint; proficiency in English

    Check how your CV matches this job

    Method of Application

    Interested and qualified? Go to Dawa Life Sciences on dawals.myadrenalin.com to apply

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