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Quality Assurance Manager (LVP Infusion Plant)
About this role
A Quality Assurance Manager is needed to oversee GMP compliance and quality for large volume parenteral IV infusion production in Ilorin, Kwara. The role targets professionals with extensive pharmaceutical production and sterile processing experience and leadership capabilities.
What you would do
- Conduct GMP self-inspections and manage CAPA plans to close non-conformities on time
- Lead or support external audits and customer audits to ensure passing and avoid deficiencies
- Maintain and improve the Quality Management System for IV infusion products
- Supervise on-site quality checks across production areas and monitor appearance, sterility and packaging quality
- Investigate deviations, quality incidents, OOS/OOT results and implement CAPAs
- Coordinate with other departments to manage quality-related matters and develop QA team capabilities
What they are asking for
- Bachelor's degree or higher in a related field (pharmacy, pharmaceutical engineering, chemistry, etc.)
- At least 3 years of team management experience in QA
- Around 10 years in pharmaceutical production and quality management, with sterile/IV infusion background
- Strong knowledge of GMP, NAFDAC regulations, sterile processing guidelines (Annex for sterile products)
- Experience with risk management, deviation investigations, and quality data analysis
- Proficiency with QMS, LIMS or similar quality informatics systems (preferred)
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