Quality Assurance Officer Makun

📌 OPPORTUNITY OVERVIEW Sagar Vitaceuticals Nigeria Limited is actively recruiting for a Quality Assurance Officer position in Makun. This is an excellent opportunity for professionals in the Pharmaceutical sector looking to advance their careers in Nigeria's dynamic job market.

🎯 IDEAL CANDIDATE PROFILE We are seeking talented individuals with the following profile: • Experience Level: 2 - 5 years • Educational Background: Bachelor or equivalent • Industry Focus: Pharmaceutical • Location Preference: in Makun

💼 WHY THIS ROLE MATTERS IN NIGERIA The Quality Assurance Officer position is an important role within Nigeria's Pharmaceutical sector, offering meaningful career development and professional growth opportunities.

📈 CAREER DEVELOPMENT INSIGHTS This role in Pharmaceutical offers valuable career progression opportunities aligned with your experience level and professional aspirations in Nigeria.

📋 APPLICATION GUIDANCE When applying for this Quality Assurance Officer position, ensure your CV highlights: • Relevant experience matching the 2 - 5 years requirement • Educational qualifications in line with Bachelor • Specific achievements in the Pharmaceutical field • Any certifications or specialized training • Proficiency in relevant software and tools

🌍 NIGERIA JOB MARKET CONTEXT The Pharmaceutical sector in Nigeria continues to show strong demand for skilled professionals. With Nigeria's growing economy and increasing foreign investment, this position represents a valuable opportunity in the current job market.

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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 Assurance Officer Paidjob posting

Location: Makun, Sagamu - Ogun

Employment Type: Full-time

Department: Quality Assurance (QA) Discover moreNiche job boardsTravel Guides & TraveloguesEmployment market analysisJob Summary

The Quality Assurance Officer ensures that all manufacturing operations, production processes, cleanroom environments, and finished products at the Sagar manufacturing facility strictly comply with cGMP, WHO, NAFDAC, and international pharmaceutical standards. This role focuses on quality systems management, batch record reviews, validation compliance, internal audits, and maintaining total quality governance across all operational stages.

cGMP & Quality Systems Governance: Implement, monitor, and enforce Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs), and quality assurance protocols across manufacturing and utility operations. Batch Document Review & Release: Review Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and analytical test results to ensure compliance before authorizing batch release. In-Process Quality Assurance (IPQA): Conduct routine line clearances, operational inspections, and environmental monitoring checks in production, packaging, and cleanroom areas. Deviations & CAPA Management: Investigate out-of-specification (OOS) results, product deviations, market complaints, and process non-conformances; design and follow up on Corrective and Preventive Actions (CAPA). Validation & Qualification Oversight: Assist in validating manufacturing processes, analytical methods, cleaning protocols, and facility equipment/HVAC qualification (IQ/OQ/PQ). Audit & Vendor Management: Participate in self-inspections (internal audits) and regulatory inspection readiness (e.g., NAFDAC, WHO); inspect incoming raw/packaging materials and assess vendor compliance. Documentation & Training: Author, review, and archive SOPs, change controls, and quality reports; conduct cGMP and QA training sessions for facility personnel.

Qualifications & Requirements

Education: B.Sc. or B.Pharm in Pharmacy, Chemistry, Biochemistry, Industrial Chemistry, or a related Life Sciences discipline. Experience: 2 - 5 years of hands-on Quality Assurance experience in a pharmaceutical manufacturing or consumer healthcare production facility. Regulatory Knowledge: In-depth working knowledge of NAFDAC regulations, WHO cGMP guidelines, ISO quality systems, and pharmaceutical validation frameworks. Core Competencies: High attention to detail, strong technical writing skills, analytical root-cause investigation skills, and audit readiness capability.

8th October, 2026. Method of Application

Interested and qualified candidates should send their CV to: [Email hidden - Login to reveal] and [Email hidden - Login to reveal] using the Job Title as the subject of the email. Paidjob posting