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Quality Assurance Manager Job in Ilorin opportunities are available for experienced professionals in pharmaceutical manufacturing and quality management. Erkang Pharmaceutical is currently recruiting a qualified Quality Assurance Manager to oversee product quality, regulatory compliance, and manufacturing standards at its facility in Ilorin, Kwara State.
The position focuses on maintaining strict quality assurance systems, ensuring compliance with Good Manufacturing Practices, and preventing contamination during the production of IV infusion products.
About Erkang Pharmaceutical
Erkang Pharmaceutical is a multinational pharmaceutical manufacturing company operating in Nigeria with production facilities in Ilorin, Kwara State.
The company is known for producing large volume parenterals and infusion products used in hospitals and healthcare facilities. Its operations follow international pharmaceutical production standards with strong emphasis on product safety, sterility assurance, and regulatory compliance.
Through advanced manufacturing technologies and strict quality systems, the organization supports the supply of pharmaceutical products to healthcare institutions.
Job Title
Quality Assurance Manager
Location
Ilorin, Kwara State, Nigeria
Employment Type
Full time
Core Objective
The Quality Assurance Manager Job in Ilorin focuses on ensuring that IV infusion production processes comply with Good Manufacturing Practices. The role aims to prevent microbial contamination, particulate contamination, and endotoxin risks while guaranteeing the quality of products released to the market.
Key Responsibilities
The responsibilities of the Quality Assurance Manager Job in Ilorin cover several areas including quality management systems, production monitoring, risk control, and supplier quality management.
Quality System Maintenance and Improvement
Establish and maintain a Quality Management System that supports the full lifecycle of IV infusion products from raw material procurement to production and market feedback.
Conduct internal GMP self inspections and mock audits to identify operational gaps and implement corrective and preventive action plans. The goal is to maintain high closure rates for quality issues.
Support official regulatory inspections and customer audits, including those conducted by National Agency for Food and Drug Administration and Control, to ensure compliance with industry regulations.
Production Process Monitoring
Perform daily inspections of IV infusion production areas including compounding, bottle washing, filling, sealing, sterilization, packaging, and visual inspection stages.
Monitor environmental conditions and personnel practices to ensure sterility standards are maintained during manufacturing processes.
Review and assess process changes related to equipment, materials, and procedures that may affect product quality.
Deviation and Risk Management
Investigate quality deviations, out of specification results, and quality incidents in order to determine root causes and implement effective corrective actions.
Conduct risk assessments for sterile pharmaceutical processes, including sterilization control, seal integrity, and prevention of particulate contamination.
Prepare annual product quality review reports and analyze production data trends related to environmental monitoring and water systems.
Materials and Supplier Quality Control
Supervise the sampling, testing, and approval of raw materials, excipients, and packaging materials used in pharmaceutical production.
Collaborate with procurement teams to evaluate supplier quality performance and conduct supplier audits when required.
Team Management and Cross Department Collaboration
Manage and train the Quality Assurance team, including system QA specialists, documentation controllers, and on site QA staff.
Coordinate with production, engineering, logistics, and procurement departments to address quality related issues and maintain compliance with regulatory standards.
Qualifications
Applicants interested in the Quality Assurance Manager Job in Ilorin should meet the following requirements.
Education
Bachelor’s degree or higher in Pharmacy, Pharmaceutical Engineering, Pharmaceutical Preparation, Biopharmacy, Chemistry, or related disciplines.
Work Experience
At least five years of professional experience in pharmaceutical manufacturing and quality management.
Candidates should also have a background in sterile pharmaceutical preparations, particularly large volume infusion production.
A minimum of three years of leadership or team management experience in quality assurance roles is required.
Professional Knowledge and Skills
Candidates applying for the Quality Assurance Manager Job in Ilorin should demonstrate knowledge and experience in the following areas.
Regulatory Compliance
Strong understanding of pharmaceutical regulations and GMP standards including sterile medicinal product requirements.
Familiarity with international sterile processing standards such as EU GMP Annex 1 or FDA sterile manufacturing guidelines is considered an advantage.
Sterility Assurance
Knowledge of IV infusion manufacturing processes including aseptic processing, autoclave validation, HVAC systems, water purification systems, and media fill testing.
Quality Investigation Tools
Experience using root cause analysis techniques such as fishbone diagrams and the 5 Why method to identify and resolve quality issues.
Information Technology Skills
Proficiency in office software and experience with digital quality management systems such as QMS or LIMS platforms.
Core Competencies
Successful candidates for the Quality Assurance Manager Job in Ilorin should demonstrate strong professional competencies including:
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High level of quality awareness and risk identification ability
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Strong communication and coordination skills across departments
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Leadership and decision making ability in high pressure production environments
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Ability to make regulatory compliant decisions related to product quality and release
Application Closing Date
The deadline for applications is 3 April 2026.
How to Apply
Interested and qualified candidates should send their CV to the official recruitment email address provided by the company.
Applications should be submitted to:
hr.erkangpharma@gmail.com
Applicants should use Quality Assurance Manager as the subject line when submitting their application.
Pharmaceutical Quality Assurance Careers
The Quality Assurance Manager Job in Ilorin offers experienced pharmaceutical professionals the opportunity to contribute to product safety and regulatory compliance in the healthcare sector.
Quality assurance roles remain essential within pharmaceutical manufacturing, ensuring that medicines meet strict safety and regulatory standards before reaching healthcare providers and patients.
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