Quality Control Personnel
Job summary
The Quality Control Personnel is responsible for ensuring that all Bioharb Global Limited products meet established quality, safety, and regulatory standards throughout the production cycle. This role oversees inspection of raw materials, in-process formulations, finished goods, and packaging to guarantee compliance with internal specifications and industry requirements. The individual will monitor production activities, implement quality testing protocols, document analytical results, and ensure strict adherence to Good Manufacturing Practices (GMP) within the company’s herbal and alternative medicine operations. The Quality Control Personnel works closely with the production, warehouse, and R&D units to maintain consistent product quality, identify deviations or defects, and drive corrective actions. This position is critical in safeguarding product integrity, strengthening customer trust, and ensuring the effectiveness, purity, and consistency of Bioharb’s health and wellness formulations.
Job descriptions & requirements
- Raw Material Quality Inspection: Verify the quality, authenticity, and suitability of all raw materials (herbs, extracts, additives, packaging materials) before accepting them into production. Ensure suppliers meet quality specifications and report any deviations immediately.
- In-Process Quality Monitoring: Inspect and document all stages of production to ensure correct formulation, measurement accuracy, mixing procedures, temperature control, and hygiene standards. Identify and flag any deviations from standard operating procedures.
- Finished Product Testing & Verification: Conduct qualitative and quantitative tests on finished products to ensure efficacy, purity, colour, texture, pH levels, and packaging accuracy meet Bioharb’s standards. Approve or reject finished batches based on test results.
- Good Manufacturing Practice (GMP) Compliance: Ensure all production activities adhere to GMP, safety, and hygiene standards. Conduct routine checks on equipment cleanliness, production floor sanitation, and staff compliance with protective gear.
- Documentation & Reporting: Maintain detailed records of inspection results, test data, batch numbers, and quality reports. Report all non-conformities and initiate corrective and preventive actions (CAPA).
- Quality Assurance Collaboration: Work closely with the Production and Warehouse teams to troubleshoot recurring issues. Participate in quality review meetings and contribute to process improvement recommendations.
- Regulatory Compliance Monitoring: Ensure products meet NAFDAC and other regulatory requirements applicable to herbal and alternative medicine products. Assist in preparing documentation for regulatory audits or product registration.
- Sampling & Laboratory Management: Collect samples for lab testing and ensure proper labelling, storage, and handling of test samples. Oversee calibration and proper use of testing equipment.
- Defect Identification & Resolution: Identify packaging defects, labelling errors, formulation inconsistencies, and product instability. Recommend immediate improvements to avoid defective batches.
- Training & Awareness: Train production staff on quality standards, hygiene practices, and compliance protocols. Reinforce adherence to quality procedures through regular coaching.
- 3-4 years of experience in a related field.
- Minimum of OND in a related field.
- Having a pharmaceutical experience is an added advantage.
- Must live around the Dopemu, Orile and Ikeja axis
Remuneration: NGN 200,000 - 300,000 Monthly
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