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  • Documentation Officer - Ogun State - Shalina Healthcare

    Shalina Healthcare
    Shalina Healthcare Ogun State

    2 months ago

    ₦900,000 - ₦1,200,000 (NGN) per year *
    Description

    About Shalina Healthcare:

    We are one of the largest, privately owned pharmaceutical businesses across Africa (Global Head Quarters- Dubai, UAE) with recent forays across multiple, new lines of businesses, viz., Digital Healthcare, Diagnostics, Consumer Healthcare, etc.

    Over the last 40 years, operating across multiple geographies, we have made it our mission to provide quality medicines to those who need it the most. We manufacture and distribute branded prescription and over-the-counter pharmaceutical and consumer products, across a broad range of therapeutic groups, including anti-malarial, antibiotics, anti-inflammatory, respiratory, gastrointestinal, nutrition, oral care, dermatology, sexual well-being, and antiseptic liquids & soaps. Leading brands, great teams and a focus on influencing the well-being of people have made Shalina a household name in Africa.

    We have a track record few can match, and our brands are among the most trusted in Africa. We are proud of our history and have big ambitions for the future. Our vision for 2030 is to be the health champion of Sub-Saharan Africa. To achieve this, we are looking for the right people to join us and create a lasting impact not just within our company but on the communities that we serve; people who identify with our Core Values and are as passionate about our Mission as we are.

    Website

    Role : Documentation Officer

    Department:
    Quality

    Location :
    Nigeria

    Job Summary

    We are looking for a Documentation Officer to join our QA team. The role involves preparing, issuing, reviewing, and controlling GMP-related documents, ensuring compliance with Good Documentation Practices (GDP), and supporting audits and inspections

    Key Responsibilities

    • Prepare, issue, and control SOPs, Batch Records, and other QA documents.
    • Maintain document master lists, revision control, and secure archiving.
    • Ensure compliance with cGMP, GDP, and regulatory requirements.
    • Support audits/inspections and coordinate document retrieval.
    • Train staff on documentation processes.

    Requirements

    • Industrial Chemistry, Microbiology, Biochemistry, Chemistry, or related field.
    • 3 -9 years' experience in QA/Documentation (Pharmaceutical or FMCG).
    • Strong knowledge of GMP/GDP and quality management systems.
    • Excellent organizational skills, attention to detail, and proficiency in MS Office.
    * This salary range is an estimation made by beBee
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