Quality Control/Assurance Manager

Quality Control/Assurance Manager

Location : Plot 6, Abimbola Way-Isolo Industrial Estate Lagos.
  • Company Jawa International Limited
  • Reports to Quality Assurance Manager & Technical Director
  • Job Type Full Time
  • Department Assurance / Compliance
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Job Overview

The Quality Control / Assurance Manager at Jawa International Limited is responsible for developing, implementing, and maintaining quality management systems to ensure full compliance with Good Manufacturing Practices (GMP), regulatory requirements, and internal quality standards. This role focuses on overseeing quality control and testing processes, regulatory compliance, audits, and continuous improvement initiatives to safeguard product quality, safety, and efficacy across the manufacturing operation.

Key Responsibilities

  1. Develop, implement, and maintain the Quality Management System (QMS) in line with GMP and regulatory requirements.
  2. Ensure compliance with NAFDAC, PCN, and other relevant regulatory body requirements and standards.
  3. Review and approve Standard Operating Procedures (SOPs), batch manufacturing records, and validation protocols.
  4. Investigate quality deviations, non-conformances, and customer complaints, and drive corrective and preventive actions (CAPA).
  5. Oversee document control, change control, and record-keeping to ensure data integrity and traceability.
  6. Coordinate staff training on GMP, quality standards, and regulatory compliance requirements.
  7. Monitor and report on quality performance metrics, and support continuous improvement initiatives.

Qualifications

Education:

  1. Sc.in Chemistry, or industrial chemistry or applied chemistry.

Experience:

  1. Minimum of 5 years’ experience in quality assurance/compliance job or as a chemical analyst / Instrumental Analyst in a pharmaceutical manufacturing company, with sound knowledge of GMP and regulatory requirements.
  2. Through knowledge of documentation in a pharmaceutical manufacturing process.

Skills and Competencies

  1. Strong knowledge of GMP, quality management systems, and pharmaceutical regulatory requirements.
  2. Excellent analytical, problem-solving, and root-cause investigation skills.
  3. Ability to work in a fast-paced, highly regulated environment.
  4. Proficient in Microsoft Office applications and quality/document management systems.
  5. Excellent communication, leadership, and interpersonal skills.

Key Attributes

  1. High level of integrity and objectivity in quality decision-making.
  2. Ability to work independently and manage time effectively.
  3. Strong commitment to GMP, safety, and regulatory compliance.
  4. Proactive in identifying compliance risks and implementing solutions.

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