Chemistry Analyst – Quality Control (QC) Department

AI summary

Dony Triump Nig. Ltd., a pharmaceutical manufacturer based in Onitsha, Anambra, is hiring a Chemistry Analyst for its Quality Control laboratory. The role involves performing chemical and instrumental analyses of raw materials, in-process samples, and finished products using HPLC, GC, UV-Vis, FTIR, and other lab instruments in line with GMP and pharmacopoeia standards. Candidates should have a BA/BSc/HND and 2–7 years of relevant experience.

• Pharmaceutical QC role focused on chemical and instrumental analysis
• Onsite full-time position in Onitsha, Anambra, Nigeria
• Requires BA/BSc/HND and 2–7 years of experience
• Involves HPLC, GC, UV-Vis, FTIR, dissolution apparatus, and other lab instruments
• GMP/GLP environment with strict documentation and data integrity requirements

Original source description

Wholly owned Nigeria company located in Onitsha, South-East Nigeria. We manufacture, and distribute Pharmaceutical products in Nigeria. We have other ancillary business that distributes wines, and PVC Chemistry Analyst – Quality Control (QC) Department Job Type Full Time , Onsite Qualification BA/BSc/HND Experience: 2 - 7 years Location Anambra Job Field Pharmaceutical , Science Department: Quality Control – Chemistry Laboratory Reports To: QC Manager / Head of Quality Control Job Purpose To perform accurate, reliable, and timely chemical and instrumental analyses of pharmaceutical materials and products in accordance with approved specifications, pharmacopoeia standards, validated analytical methods, SOPs, and applicable GMP requirements. Key Responsibilities: Laboratory Analysis The Chemistry Analyst shall: Collect and/or receive samples submitted to the QC laboratory. Perform analysis of raw materials, packaging materials, in-process samples, finished products, stability samples and water samples, as assigned. Carry out chemical tests such as: Identification tests Assay/potency pH Dissolution Disintegration Related substances/impurities Moisture/water content Loss on drying Specific gravity Viscosity Titrations Limit tests Other applicable physicochemical tests. Operate laboratory instruments such as: HPLC GC UV-Visible spectrophotometer FTIR Dissolution apparatus pH meter Karl Fischer apparatus Analytical balances Other approved laboratory equipment. GMP and Documentation Follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) at all times. Perform laboratory activities strictly according to approved SOPs and analytical methods. Accurately record all observations, calculations, results and instrument readings. Complete laboratory worksheets, analytical reports, logbooks and other QC documentation. Ensure ALCOA+ principles are maintained for laboratory data integrity. Ensure that raw data are attributable, legible, contemporaneous, original/true copies, accurate, complete, consistent, enduring and available. Report any discrepancy, abnormal result or suspected data-integrity issue immediately to the supervisor. Instrument and Equipment Management Operate laboratory instruments correctly and safely. Perform routine checks and basic maintenance of laboratory equipment. Ensure instruments are within their calibration/qualification period before use. Record equipment usage in appropriate logbooks. Report malfunctioning or damaged equipment promptly. Assist with calibration, qualification and preventive maintenance activities when required. Reagents and Standards Prepare and standardize laboratory reagents and solutions according to approved procedures. Properly label prepared reagents with preparation date, expiry/retest date, concentration and other required information. Maintain appropriate records for reagents and reference standards. Ensure reference standards are stored and handled according to approved requirements. Dispose of expired reagents and chemical waste safely and according to established procedures. OOS/OOT Investigations Immediately notify the QC supervisor/manager of Out-of-Specification (OOS) or Out-of-Trend (OOT) results. Participate in laboratory investigations of atypical, erroneous or unexpected results. Assist in identifying possible laboratory errors and determining appropriate corrective actions. Do not repeat or invalidate an analysis without authorization and documented justification. Sampling and In-Process Testing Where assigned, the analyst may: Assist with sampling of raw materials and finished products. Perform in-process testing during manufacturing. Analyze samples from blending, granulation, compression, coating, filling or other production stages. Communicate test results promptly to authorized personnel to support manufacturing decisions. Safety and Housekeeping Handle chemicals, solvents and pharmaceutical samples safely. Wear appropriate PPE at all times. Follow laboratory safety procedures and chemical-handling requirements. Maintain cleanliness and organization of the laboratory. Ensure chemical spills, breakages and other laboratory incidents are immediately reported. Participate in laboratory waste segregation and disposal. Quality and Compliance Responsibilities: The Chemistry Analyst must: Maintain strict independence and objectivity when reporting analytical results. Never manipulate, fabricate, backdate or selectively report laboratory data. Ensure only approved and current SOPs/methods are used. Participate in internal audits, regulatory inspections and QC investigations when required. Assist with method validation, verification, transfer and analytical method development where applicable. Participate in CAPA implementation and effectiveness checks where assigned. Maintain confidentiality of company, product and analytical information. Daily Activities A typical day may include: Sample receipt → Sample preparation → Instrument/equipment checks → Analysis → Calculations → Result verification → Documentation → Review/submission of results → Laboratory housekeeping The analyst should prioritize accuracy and data integrity over speed. A fast result that is unreliable or inadequately documented is not acceptable in pharmaceutical QC. Check how your CV aligns with this job Method of Application Interested and qualified candidates should apply using the Apply Now button below. Build your CV for free. Download in different templates.