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  • Posted: Apr 23, 2024
    Deadline: Apr 30, 2024
  • Never pay for any CBT, test or assessment as part of any recruitment process. When in doubt, contact us

    CREM is a service provider in the areas of Research & Development, Learning & Development, Consulting, Entrepreneurship Solutions, and Outsourcing Services across Nigeria and Africa. We equip Organization’s Human Resources with skills, competencies and performance improving capacities. CREM is driven by People, Process, Technology and Service to e...
    Read more about this company




    • Microbial analysis of raw materials.
    • New sampling of materials
    • Preparation of media for microbial analysis
    • Microbial analysis of finished, bulk and intermediate
    • Proper documentation of records.
    • Fumigation of the factory.
    • Carrying out an environmental check (air sampling)
    • Calibrate or maintain Laboratory equipment
    • Complete documentation needed to support testing procedures including equipment Log books or inventory forms.
    • Maintaining GLP in the Laboratory.
    • Instrumental and Microbiological Analysis.


    • Both Freshers and experienced persons will be considered.
    • For experienced persons, work experience of more than 1 year to 2 year is ideal.

    go to method of application »

    Compliance Officer


    • Conduct regular inspections and monitoring of in-process manufacturing activities to ensure compliance with Good Manufacturing Practices (GMP) and other regulatory requirements
    • Collaborate with production teams to identify and address any deviations from quality standards
    • Review and verify the accuracy and completeness of in-process
    • documentation, batch records and related manufacturing records.
    • Ensure that all documentation complies with established procedures and regulatory guidelines
    • Work closely with the quality control team to implement in-process quality checks
    • Collaborate on the resolution of quality-related issues and deviations, providing support for investigations
    • Provide training to manufacturing personnel on in-process compliance requirements, quality standards and regulatory expectations
    • Promote a culture of awareness and accountability for in-process compliance within the manufacturing teams
    • Identify opportunities for process improvements andoptimizationn of in-process compliance procedures
    • Implement corrective and preventive actions to enhance overall compliance performance
    • Stay updated on relevant regulations and guidelines impacting pharmaceutical manufacturing
    • Ensure that manufacturing processes align with current regulatory expectations

    Qualification and experience:

    • Candidates with a Science background will only be considered.
    • HND/OND/B.Sc. in any of the subjects like PURE / INDUSTRIAL/APPLIED CHEMISTRY or MICROBIOLOGY, BIOCHEMISTRY / FOOD SCIENCE/PHYSICAL SCIENCE are candidates we are looking for.
    • Freshers with exceptional qualities that can be developed to fit into the post will also be considered.
    • 1 to 2 years experience in a similar field of job or experience as
    • COMPLIANCE OFFICER in any process/manufacturing company will be
    • considered for the experience category.
    • Computer operation knowledge is an added advantage

    go to method of application »

    Raw Material Supervisors

    Job description:

    • Individuals shall be able to take care of the incoming raw materials to our stores and inventory management and proper record keeping.
    • Responsible for issuing our materials to the user department and keeping and updating the relevant records.


    • Candidates should have a science background
    • Basic knowledge of Computer operation and MS Office operating knowledge.
    • Fresher or experienced candidates are required
    • Any inventory management software working knowledge is an additional advantage.

    Educational Qualification:

    • OND/HND/B.Sc from any Science background.
    • Any qualification in computer course will be an added advantage


    • A minimum of 0 to 2 years experience in a raw materials job, especially in a warehouse/depot or in a manufacturing industry.


    • Supervision of raw materials for Pharmaceutical production process and manpower .
    • Proper reporting and stock taking
    • Coordination of the raw materials department for the required process
    • Checks to be carried out from time to time.


    • Dynamic
    • Adaptability
    • Communication.

    Method of Application

    Interested and qualified candidates should send their CV to: using the Job Title as the subject of the mail.

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