Quality Compliance Assistant Manager

Willers Solutions

Job Overview

Location

Lagos, Lagos, Nigeria

Employment Type

Full-time

Work Arrangement

On-site

Sector

Engineering & Manufacturing

Experience Level

Mid-level (3-5 years)

Application Deadline

April 30, 2026

Job Description

Willers Solutions is seeking a Quality Compliance Assistant Manager to oversee quality assurance protocols at a pharmaceutical manufacturing plant in Lagos.

This role is crucial for ensuring that all manufacturing processes align with regulatory standards, maintaining rigorous documentation, and upholding cGMP requirements.

Key responsibilities include ensuring strict adherence to NAFDAC rules and cGMP standards, preparing and managing QA/QC documentation, monitoring production processes for quality deviations, and assisting in quality audits. You will utilize MS Office to track quality metrics and submit detailed compliance reports.

To apply for this role, click the Apply button on this page and follow the instructions.

Required Skills

NAFDAC RegulationscGMP StandardsQA/QC DocumentationCompliance ReportingMS OfficeAttention to DetailInvestigative Skills

Key Responsibilities

  • Ensure all plant operations strictly adhere to NAFDAC rules, regulations, and cGMP standards.
  • Prepare, review, and manage comprehensive QA/QC documentation, including SOPs and compliance reports.
  • Monitor production processes to identify and resolve quality deviations.
  • Assist in internal and external quality audits to maintain industry certifications.
  • Utilize MS Office to track quality metrics and submit detailed compliance reports to management.

Qualifications

  • HND or Bachelor’s degree in any Science discipline.
  • Minimum of 5 years in a QA/QC role within a reputable pharmaceutical, food, or process manufacturing industry.
  • Thorough understanding of NAFDAC regulations and cGMP guidelines is mandatory.
  • Proficiency in MS Office (Word, Excel, Outlook) is a must.
  • Strong attention to detail, investigative skills, and expert knowledge of documentation procedures.

How to Apply

Use “Quality Compliance Assistant Manager” as the subject of the email.

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The Nigerian pharmaceutical manufacturing sector is under stringent regulatory oversight, with a growing emphasis on cGMP compliance and quality assurance. This Quality Compliance Assistant Manager role is critical for upholding these standards. Key technical skills include NAFDAC regulations, cGMP guidelines, QA/QC documentation, and data analysis using MS Office. Your leadership will ensure product safety and efficacy, directly impacting consumer trust and the company's reputation in a highly regulated industry.

Posted Date

April 15, 2026