Job Description
A reputable pharmaceutical manufacturing company is seeking an experienced Quality Assurance Executive to support quality management systems and ensure pharmaceutical products consistently meet regulatory and quality standards. This role is ideal for professionals with extensive experience in pharmaceutical quality assurance, GMP compliance, documentation control, and manufacturing quality processes.
Key Responsibilities
- Ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and applicable regulatory requirements, including NAFDAC and WHO guidelines.
- Monitor manufacturing and packaging operations to ensure all processes follow approved quality procedures.
- Review batch manufacturing records, batch packaging records, and other quality documents for accuracy, completeness, and compliance.
- Perform line clearance activities before and after production while carrying out in-process quality inspections.
- Participate in internal audits, external audits, and regulatory inspections.
- Maintain quality documentation, specifications, SOPs, and quality records while promoting Good Documentation Practices (GDP).
Requirements
- Bachelor’s Degree (B.Sc. or HND) in Pharmacy, Microbiology, Biochemistry, Chemistry, or a related science discipline.
- Professional certification or membership with a relevant regulatory body is an added advantage.
- Minimum of 5–8 years of experience in a pharmaceutical manufacturing environment.
- Strong knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and pharmaceutical regulatory requirements.
- Experience with documentation review, deviation management, CAPA, validation, risk management, and audit processes.
- Proficiency in Microsoft Office applications, including Excel, Word, and PowerPoint.