QUALITY ASSURANCE SUPERVISOR AT CHRIS EJIK GROUP OF COMPANIES | QUALITY ASSURANCE JOBS IN LAGOS

About Company:

Incorporated in 1987, Chris Ejik Group is a multi dimensional company with interest in Power Generation & Transmission, Pharmaceutical & Healthcare Products, Electronics, and Agro Allied Products. Carving a niche for itself, Chris Ejik Group and its subsidiaries operates in several sectors of the Nigerian economy and is on the move to cover more grounds.

Job Description:

We are seeking a structurally elite and operationally rigorous Quality Assurance Supervisor to anchor the quality immune system and regulatory engine of our pharmaceutical operations. In a high-stakes clinical landscape where institutional momentum is dictated by the velocity of the production-cycle and the precision of the bio-safety filter success is defined by "Quality Sovereignty" the ability to harmonize complex regulatory frameworks (GMP/ISO/NAFDAC) with the clinical precision required for Root Cause Analysis (CAPA), Audit Readiness, and Production-Line Fidelity. This role is designed as a "Quality Launchpad" a critical mission for an expert supervisor who can blend "Quality Grit" (mastering the complexities of pharmaceutical inspection and remediation) with the "Structural Agility" required to execute High-Fidelity Compliance Workflows.

Requirements:

1. Orchestration & Quality Governance

• Sovereignty of the Standard: Supervise the QA team and monitor production processes to ensure adherence to quality policies, acting as the primary "Source of Quality Throughput."

• Regulatory Architecture: Ensure total compliance with NAFDAC, cGMP, and ISO standards, providing the "Structural Foundation" for licensure and audit success.

• Integrity Stewardship: Conduct rigorous inspections and audits on raw materials and finished products, ensuring the "Source of Institutional Safety" is elite and uncompromised.

2. Tactical Resilience & Analytical Logic

• Risk Sovereignty: Investigate quality issues, identify root causes, and implement corrective/preventive actions, acting as the primary "Source of Risk-Mitigation Strategy."

• Documentation Architecture: Maintain precise quality records and reports, providing the "Functional Foundation" for regulatory traceability.

• Collaboration Stewardship: Integrate with production and external teams to improve product quality, maintaining the "Source of Operational Continuity."

3. Operational Integrity & Performance Power

• Capability Sovereignty: Train and mentor QA staff on best practices, acting as the primary "Source of Team Technical Competency."

• Process Architecture: Utilize Quality Management System (QMS) Toolkits to track compliance performance, providing the "Relational Foundation" for data-driven quality decisions.

• Velocity Logic: Utilize Pharmaceutical expertise to accelerate the "Detection-to-Correction" cycle, maximizing the "Source of Production Momentum."

Qualifications and Skills:

Professional Profile

• Education: Bachelor’s degree in Quality Management, Chemistry, Microbiology, Industrial Engineering, or related fields.

• Experience: Minimum of 3–5 years of hands-on QA experience, ideally in the manufacturing or pharmaceutical industry.

• Technical Power: Deep knowledge of cGMP, ISO standards, and NAFDAC regulatory requirements.

• Aptitude: Exceptional analytical skills, meticulous attention to detail, and the leadership capacity to drive quality culture across production departments.

• Mindset: Proactive, disciplined, and capable of maintaining "Quality Sovereignty" under high-pressure production deadlines.

Core Competencies

• Quality Grit: Ability to identify, isolate, and remediate quality discrepancies before they compromise product safety.

• Regulatory Sovereignty: Mastery of the "Inspect-Validate-Train-Audit-Remediate" lifecycle.

• Execution Power: High-discipline approach to QMS maintenance, regulatory documentation, and the consistent delivery of compliant pharmaceutical outputs.

Salary

Application Closing Date: 30th April, 2026

Application Instructions:

Interested and qualified candidates should forward their CV and a link to their portfolio to: career@chrisejik.com using the position as subject of email.