Pharmacist at Sagar Vitaceuticals Nigeria Limited

Company: Sagar Vitaceuticals Nigeria Limited Location: Nigeria State: Ogun Jobs Job type: Full-Time Job category: Healthcare/Medical Jobs in Nigeria Sagar Vitaceuticals Nigeria Limited (SVNL) is a pharmaceutical manufacturing company based in Ikeja, Lagos. Originally established as a joint venture, it is now owned by Sagar Overseas Ltd. SVNL operates a modern facility with high-capacity production lines for tablets, capsules, ointments, and more, adhering to GMP standards. The company is NAFDAC-approved and partners with Nigeria’s Federal Ministry of Health to support local drug production. Its product portfolio includes vitamins, antibiotics, and over-the-counter supplements. We are recruiting to fill the position below: Job Title: Pharmacist Location: Ogun Department: Production Reports To: Pharmaceutical Manager / Quality Manager / Production Manager Job Summary The Pharmacist is responsible for supporting the development, manufacturing, quality assurance, regulatory compliance, and distribution of pharmaceutical products. The role ensures that all products meet regulatory requirements, Good Manufacturing Practice (GMP) standards, and company quality policies while promoting patient safety and product effectiveness. Job Description A pharmacist in a pharmaceutical company is responsible for ensuring that medicines are developed, manufactured, tested, stored, and distributed in compliance with regulatory standards while maintaining product quality, safety, and efficacy. Key Responsibilities Ensure compliance with Good Manufacturing Practice (GMP), Good Distribution Practice (GDP), and applicable pharmaceutical regulations. Supervise and monitor the manufacturing process to ensure products meet quality standards. Review and approve batch manufacturing and packaging records. Conduct quality assurance and quality control activities, including reviewing test results and investigating deviations. Monitor product stability and ensure proper storage and handling of pharmaceutical products. Prepare and maintain accurate documentation in accordance with regulatory requirements. Participate in internal and external audits and implement corrective and preventive actions (CAPA). Support product registration, licensing, and regulatory submissions. Investigate customer complaints, product defects, and recalls when necessary. Provide technical guidance and training to production and quality personnel. Collaborate with research and development, production, engineering, and regulatory teams during product development and commercialization. Ensure compliance with health, safety, and environmental policies. Keep up to date with changes in pharmaceutical regulations and industry best practices. Key Performance Indicators (KPIs) Compliance with GMP and regulatory standards. Reduction in manufacturing deviations and quality incidents. Successful completion of audits with minimal observations. Timely completion of documentation and batch record reviews. Product quality and customer satisfaction. Effective implementation of corrective and preventive actions (CAPA). Required Qualifications Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D.). Valid pharmacist license / registration with the appropriate regulatory authority. Experience in pharmaceutical manufacturing, quality assurance, quality control, or regulatory affairs is preferred. Knowledge of GMP, GDP, GLP, and pharmaceutical quality systems. Strong analytical and problem – solving skills. Excellent communication and teamwork abilities. Proficiency in Microsoft Office and pharmaceutical documentation systems. Key Skills: Pharmaceutical manufacturing. Quality assurance and quality control. Regulatory compliance. Documentation and record management. Risk assessment and problem-solving. Attention to detail. Time management. Leadership and teamwork. Communication and presentation skills. Working Conditions Work is primarily performed in manufacturing plants, laboratories, offices, or warehouse environments. May require the use of personal protective equipment (PPE). May involve shift work depending on production schedules. Application Closing Date 31st July, 2026. Don't Keep! Kindly

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