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  • Posted: Dec 7, 2022
    Deadline: Dec 22, 2022
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    Incorporated in 1987, Chris Ejik Group is a multi dimensional company with interest in Power Generation & Transmission, Pharmaceutical & Healthcare Products, Electronics, and Agro Allied Products. Carving a niche for itself, Chris Ejik Group and its subsidiaries operates in several sectors of the Nigerian economy and is on the move to cover more grou...
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    Quality Assurance Officer

    Responsibilities

    • Lead root cause analysis and corrective and preventive actions for audit observations, product complaints, product non-conformances, in-process deviations issues related to process controls
    • Review completed batch records and other cGMP documents to ensure accuracy and completion in accordance with cGMP regulations
    • Write, review and modify, as needed, SOPs for compliance with appropriate regulations
    • Prepare/revise operating procedures and specifications
    • Review/approve routine change control requests, deviation, quality risk assessment as designated
    • Review and approve suppliers / service providers including supporting with audits of critical suppliers where required
    • Monitor and ensure that batch records are audited per manufacturing/packaging/shipping requirements, when required.
    • Lead and perform data review audits (Batch Production Records, Validation Documents and Development Documentation, Quality Control Data as required)
    • Document non-compliance and evaluate if further investigation is needed
    • Document results of deviation and complaint investigations, analysis, corrective actions and preventive actions
    • Maintain quality records (equipment calibration and maintenance, training, deviation and complaint investigation, environmental monitoring, Certificate of Analysis, clean room certification etc.)
    • Assist in incident investigation and reporting
    • Assist in preparation and reviewing of key quality documents like SMF, Quality manual, Validation Master Plan, protocols and report

    Qualifications

    • Bachelor's Degree in Biological Sciences, Chemistry or related discipline, or equivalent relevant cGMP work experience.
    • Minimum of 2 years relevant pharmaceutical industry experience in a cGMP environment
    • Ability to comply with all good manufacturing practices (GMPs) regulations and follow all standard operating procedures (SOPs).
    • Proficiency with Microsoft Office suite with emphasis on Word and excel
    • Knowledge of tools, concepts and methodologies of QA
    • Solid experience in effective usage of data analysis tools and statistical analysis
    • Ability to multitask and manage time effectively to ensure all work streams are managed.
    • Must possess excellent communication skills
    • Abilityto solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.

    Method of Application

    Interested and qualified candidates should send their Curriculum Vitae and Cover Letter to: careers@chrisejik.com using the Job Title as the subject of the email.

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