Quality Control Officer
AI summary
Sagar Vitaceuticals Nigeria Limited is hiring a Quality Control Officer in New Makun City, Ogun State. The role involves testing raw materials, in-process and finished pharmaceutical products, maintaining laboratory equipment, and ensuring compliance with GMP, GLP, and NAFDAC regulations. Full-time position.
- Full-time Quality Control Officer role in Ogun State
- Pharmaceutical testing and laboratory operations
- GMP, GLP, and NAFDAC compliance responsibilities
- HPLC, UV-Vis, and dissolution testing experience valued
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- UnclearRelated work experienceThe text mentions experience, but the exact level should be confirmed at source.
- PreferredPractical evidence in internship, Quality Control, LaboratoryThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
- UnclearComfort with the Full-time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Quality Control Officer evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Sagar Vitaceuticals Nigeria Limited and the role in Not specified.
- Add concrete examples related to internship, Quality Control, Laboratory, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Jobzilla Nigeria; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
Source and safety check
- Jobzilla Nigeria
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Quality Control Officer role in internship, Quality Control?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Sagar Vitaceuticals Nigeria Limited before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
Quality Control Officer at Sagar Vitaceuticals Nigeria Limited ⏲ Aug 21, 2026, 8:03 AM ⋕ View all Pharmaceutical jobs Sagar Vitaceuticals Nigeria Limited formerly known as Strides Vital Nigeria Limited was a strategic partnership comprising Vital Pharmaceuticals Ltd and India’s Strides Arcolabs Ltd,a NSE listed company. In 2017, Management of Sagar Overseas Limited, acquired 100% shares in Strides Vital Nigeria Limited and the company was re-named to Sagar Vitaceuticals N... We are recruiting to fill the position below: Job Title: Quality Control Officer Location: New Makun City Ogun Employment Type: Full-time Job Summary A Quality Control (QC) Officer is responsible for ensuring that raw materials, in-process materials, finished pharmaceutical products, packaging materials, and laboratory processes meet approved quality specifications and regulatory requirements: before products are released for use or sale. Key Responsibilities: Raw Material Testing: Perform identification, assay, purity, pH, moisture and other applicable tests. Verify results against approved specifications. Collect and analyze samples of active pharmaceutical ingredients (APIs), excipients, and other raw materials. In-Process and Finished Product Testing: Analyze products during and after manufacturing. Ensure results comply with established specifications. Carry out tests such as: Weight variation pH Hardness Dissolution Assay Microbial limits, where applicable. Friability Disintegration Laboratory Operations: Perform routine laboratory checks and maintain equipment records. Ensure instruments are properly calibrated and suitable for use. Operate and maintain laboratory equipment such as HPLC, UV-Visible spectrophotometer, dissolution apparatus, friabilator, disintegration tester, pH meter and analytical balances. Documentation: Prepare Certificates of Analysis (CoAs), where assigned. Maintain proper documentation in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Accurately record analytical results in laboratory notebooks, worksheets, logbooks and electronic systems. Deviation and OOS Investigation: Assist with corrective and preventive actions (CAPA). Identify and report Out-of-Specification (OOS) and Out-of-Trend (OOT) results. Participate in investigations to determine the root cause of abnormal results. Sampling: Perform or assist with sampling of raw materials, packaging materials, in-process products and finished products according to approved procedures. Ensure samples are properly labelled, stored and documented. Compliance and Quality Systems: Participate in internal and external audits when required. Follow approved Standard Operating Procedures (SOPs) and laboratory safety procedures. Support compliance with GMP, GLP, pharmacopoeial requirements: and NAFDAC regulations. Stability Studies: Monitor samples stored under specified conditions and document analytical results over time. Assist with stability testing of pharmaceutical products. Laboratory Safety: Ensure proper storage, labelling and disposal of chemicals and laboratory waste. Handle chemicals, reagents and pharmaceutical samples safely. Follow relevant occupational health and safety requirements. Typical Qualifications For a QC Officer position, companies commonly look for: Knowledge of pharmaceutical analytical techniques Knowledge of GMP and GLP Good attention to detail and ability to work according to SOPs Experience: with laboratory instruments, particularly HPLC and UV-Vis, is an advantage Ability to interpret analytical results Good documentation and record-keeping skills B.Sc./B.Tech in Chemistry, Biochemistry, Pharmacy, Pharmaceutical Chemistry, Microbiology or a related discipline Technical skills: Analytical chemistry Assay determination Pharmaceutical microbiology, depending on the QC section UV-Vis spectroscopy Laboratory equipment calibration. Titration HPLC analysis Dissolution testing Data interpretation Professional skills: Attention to detail Good documentation Accuracy Integrity and adherence to procedures. Teamwork Time management Problem-solving In a company like Sagar Vitaceuticals: If you're preparing specifically for a QC Officer interview at Sagar Vitaceuticals Nigeria Limited, you should be particularly comfortable discussing tablet/capsule analysis, GMP, HPLC, assay, dissolution, disintegration, friability, hardness, OOS investigations, SOPs, sampling, documentation and NAFDAC requirements. Salary N150,000 - N220,000 per month. How to Apply Interested and qualified candidates should send their CV to: nosa@svnl.in using the Job Title as the subject of the email. Application Deadline: 30th September, 2026. View all Jobs in Nigeria Ogun State Quality Control Officer job vacancies in Nigeria