Global Linkers Limited - We are forward-thinking HR consulting firm dedicated to partnering with upcoming and medium-scale businesses to strengthen their people practices and achieve sustainable growth. We provide practical, cost-efficient HR solutions that streamline operations, enhance workforce capability, and allow business leaders to stay focused on their core priorities. By reducing administrative burden and improving productivity, we support organizations in unlocking their full potential with confidence and professionalism.
We are recruiting to fill the position below:
Job Title: Quality Assurance Manager
Location: Calabar, Cross River
Job Summary
The Quality Assurance Manager is responsible for establishing, implementing, and maintaining the company's Quality Management System (QMS) to ensure that all pharmaceutical manufacturing activities comply with GMP, regulatory requirements, approved procedures, and established quality standards.
The role provides oversight of quality systems, documentation, batch release processes, deviations, CAPA, validation, audits, and continuous quality improvement.
Key ResponsibilitiesLead and manage the Quality Assurance function and ensure effective implementation of the company's QMS.
Ensure manufacturing, packaging, storage, and related activities comply with GMP and approved SOPs.
Review and approve Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), SOPs, specifications, and other quality documents.
Oversee investigations of deviations, non-conformances, complaints, and out-of-specification results in collaboration with relevant departments.
Manage CAPA, change control, risk assessment, and quality improvement activities.
Ensure effective line clearance and in-process quality assurance activities.
Coordinate product, process, equipment, and cleaning validation activities.
Monitor environmental, hygiene, and facility-related quality requirements where applicable.
Coordinate internal, supplier, and regulatory inspections/audits and ensure timely closure of findings.
Ensure proper management of controlled documents, records, and quality-related data.
Work closely with QC, Production, Warehouse, Engineering, PPIC, and Regulatory Affairs to resolve quality issues.
Support investigation and resolution of product complaints, returns, recalls, and quality incidents.
Monitor compliance with GMP requirements and provide appropriate training to employees.
Maintain quality metrics and prepare periodic QA reports for Management.
Identify quality risks and recommend preventive and corrective measures.
Promote a strong culture of quality, compliance, accountability, and continuous improvement across the organisation.
RequirementsDegree in Pharmacy, Chemistry, Biochemistry, Microbiology, Pharmaceutical Sciences/Technology, Pharmacology/Toxicology, Chemical Engineering or related scientific discipline.
Minimum of 7 years' pharmaceutical manufacturing experience, with at least 3 years in QA supervision/management.
Strong practical experience in GMP, QA systems, batch documentation, CAPA, deviations, validation and regulatory inspections.
Application Closing Date18th September, 2026.
How to Apply
Interested and qualified candidates should send their updated CV to: [Email hidden - Login to reveal] using "Quality Assurance Manager" as the subject of the email.
How To Apply
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Make sure to send your application before the closing date.
Note: Only shortlisted candidates are contacted.
