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  • Posted: Aug 20, 2025
    Deadline: Not specified
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  • Shalina Healthcare is a market leader in making quality healthcare products affordable and available across Africa. We achieve this by sourcing from WHO-approved production facilities in India and China and by focusing on our first-class distribution expertise. Shalina Healthcare is privately owned and part of the Shalina Group. We have been operating in...
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    IPQC Officer

    Job Summary:

    • To ensure that in-process materials and production processes comply with GMP standards and defined specifications by carrying out routine inspections and sampling during production activities.

    Key Responsibilities

    • Conduct in-process quality checks on manufacturing activities including granulation, compression, coating, filling, and packaging processes.
    • Monitor critical process parameters and ensure adherence to approved batch manufacturing records (BMR) and standard operating procedures (SOPs).
    • Perform sampling and testing of in-process materials (e.g., weight variation, hardness, friability, disintegration time, leak test, etc.).
    • Ensure line clearance before the start of any batch or product changeover.
    • Report any deviations or non-conformities observed during the process to the QA/QC Supervisor or Manager.
    • Ensure proper segregation, labeling, and handling of in-process and intermediate materials.
    • Maintain accurate and timely documentation of observations and test results.
    • Assist in the investigation of process deviations and support CAPA implementation.
    • Ensure compliance with cGMP, safety, and hygiene standards during operations.
    • Participate in routine training on GMP and SOPs.
    • Support continuous improvement initiatives in quality and production operations.

    Qualifications and Experience

    • B.Sc / HND in Chemistry, Biochemistry, Microbiology, Industrial Chemistry, or related science discipline.
    • 1–3 years of experience in IPQC or a related quality role in a pharmaceutical manufacturing environment.
    • Good knowledge of cGMP, in-process testing procedures, and pharmaceutical manufacturing operations.
    • Familiarity with regulatory requirements (e.g., NAFDAC, PCN is an advantage.

    Key Skills & Competencies

    • Strong attention to detail and observation skills.
    • Ability to work independently and as part of a team.
    • Excellent written and verbal communication.
    • Good documentation and record-keeping skills.
    • Ability to work under pressure and in a fast-paced environment.
    • Proficient in MS Office applications (Word, Excel, etc.).

    Check how your CV aligns with this job

    Method of Application

    Interested and qualified candidates should send a recent copy of their CV to: recruitment.diagnostics@shalina.com using the Job Title as the subject of the email.

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