What Quality Assurance Specialist Jobs are in Nigeria?

Our client, a renowned pharmaceutical company committed to producing high-quality medicines, is seeking a dedicated Quality Assurance Specialist to join their team in Abeokuta, Ogun, NG . This role is essential for maintaining and improving our quality management system, ensuring compliance with regulatory standards, and overseeing all aspects of quality assurance in pharmaceutical operations. The ideal candidate will have a strong understanding of QA principles, experience in the pharmaceutical industry, and a meticulous approach to quality control. This hybrid position offers a blend of in-office collaboration and remote flexibility, providing a balanced work environment. Join a team focused on upholding the highest standards of quality in pharmaceutical production.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with GMP and other applicable regulations.
• Conduct internal audits and support external audits by regulatory agencies and customers.
• Review and approve batch records, validation protocols, and other quality-related documents.
• Manage deviation investigations, CAPA (Corrective and Preventive Actions), and change control processes.
• Ensure compliance with all relevant regulatory requirements, including local and international pharmaceutical standards.
• Participate in supplier qualification and monitoring activities.
• Train personnel on quality assurance procedures and GMP principles.
• Monitor quality metrics and prepare reports for management review.
• Contribute to the continuous improvement of quality processes and systems.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and regulatory requirements.
• Experience with internal audits, deviation management, and CAPA implementation.
• Strong analytical and problem-solving skills.
• Excellent written and verbal communication skills.
• Proficiency in quality management software and standard office applications.
• Detail-oriented and highly organized.
• Ability to work effectively both independently and as part of a team in a hybrid work environment.

Our client offers a competitive salary and a comprehensive benefits package, including health insurance, retirement plans, and paid time off. The hybrid work model provides flexibility and a good work-life balance. Opportunities for professional development, training, and career advancement within a growing pharmaceutical company are readily available. Join our dedicated quality team in Abeokuta, Ogun, NG and contribute to the delivery of safe and effective medicines.

Our client, a prominent pharmaceutical company committed to excellence, is seeking a diligent and proactive Quality Assurance Specialist to join their dedicated team in Gombe, Gombe . This role is fundamental in ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, in full compliance with regulatory requirements. The successful candidate will be responsible for implementing and maintaining the quality management system, conducting audits, and driving continuous improvement initiatives. This is an essential on-site position, requiring active participation in quality control and assurance processes at our Gombe, Gombe facility.

• Implement and maintain the Quality Management System (QMS) in accordance with cGMP and other relevant regulations.
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Review and approve batch records, validation documents, and change controls.
• Investigate deviations, customer complaints, and out-of-specification results, and ensure timely resolution.
• Participate in external audits by regulatory agencies and customers.
• Develop and deliver quality assurance training to relevant personnel.
• Monitor key quality metrics and prepare quality reports for management review.
• Ensure compliance with all applicable regulatory requirements (e.g., NAFDAC, FDA, EMA).
• Contribute to the continuous improvement of quality systems and processes.
• Manage product release activities, ensuring all requirements are met prior to market distribution.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 3 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• Strong understanding of cGMP, ICH guidelines, and other relevant regulatory standards.
• Experience in auditing, deviation management, CAPA, and change control processes.
• Excellent analytical, problem-solving, and critical thinking skills.
• Detail-oriented with strong organizational and documentation skills.
• Effective communication and interpersonal skills, with the ability to interact with various departments and external stakeholders.
• Proficiency in Microsoft Office Suite and familiarity with quality management software.
• Ability to work independently and as part of a team in a fast-paced environment.
• Commitment to upholding the highest standards of quality and compliance in Gombe, Gombe .

Our client offers a competitive salary, comprehensive health benefits, and opportunities for professional development and career advancement. Employees benefit from working within a company that prioritizes quality and patient safety, contributing to the development of essential medicines. The role provides a chance to make a tangible impact on product quality and regulatory compliance. This position is located in Gombe, Gombe , offering a stable and rewarding career path within the pharmaceutical sector.

Our client, a respected pharmaceutical manufacturer, is seeking a meticulous and experienced Quality Assurance Specialist to join their dedicated team in Enugu . This position is integral to maintaining the highest standards of quality and compliance throughout the pharmaceutical manufacturing process. The successful candidate will play a key role in implementing and overseeing quality systems, ensuring adherence to regulatory requirements, and supporting continuous improvement initiatives. This is an excellent opportunity to contribute to patient safety and product integrity within a company that prioritizes quality and ethical practices.

• Implement and maintain the company's Quality Management System (QMS) in compliance with regulatory standards (e.g., GMP, ISO).
• Conduct internal audits of manufacturing processes, quality control procedures, and documentation to ensure compliance.
• Review and approve batch records, specifications, and other quality-related documents.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, determining root causes and implementing corrective and preventive actions (CAPAs).
• Participate in external audits by regulatory authorities and customers, coordinating responses and follow-up actions.
• Develop, implement, and deliver training programs on quality assurance principles and GMP requirements to relevant personnel.
• Monitor and analyze quality metrics and trends, reporting findings and recommending improvements.
• Contribute to process validation activities and ensure that all manufacturing processes are validated and operating within established parameters.
• Manage change control processes, ensuring that all changes to products, processes, or equipment are adequately assessed and documented.
• Support the qualification and validation of equipment and facilities.
• Liaise with Quality Control, Production, and Regulatory Affairs departments to ensure integrated quality oversight.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 4 years of experience in pharmaceutical Quality Assurance or Quality Control.
• Thorough understanding of GMP regulations and quality management systems.
• Experience in conducting internal audits, handling deviations, OOS investigations, and CAPA management.
• Knowledge of validation principles (process, equipment, cleaning) is required.
• Strong analytical, problem-solving, and decision-making skills.
• Excellent attention to detail and organizational abilities.
• Proficiency in documentation and report writing.
• Effective communication and interpersonal skills, with the ability to interact professionally with all levels of staff and external auditors.
• Familiarity with Quality Risk Management principles is an advantage.

Our client offers a competitive salary, comprehensive health insurance, and opportunities for professional development and career growth. Employees benefit from a supportive work environment, access to modern facilities, and the satisfaction of contributing to the production of high-quality pharmaceuticals that improve health outcomes. Generous annual leave and ongoing training are also provided.

• Lead and manage the automotive quality assurance team, providing guidance and supervision.
• Develop, implement, and maintain the company's quality management system (QMS) in accordance with industry standards (e.g., IATF 16949).
• Establish and monitor quality control procedures throughout the manufacturing process, from raw materials to finished goods.
• Conduct regular internal audits of production processes and quality control measures.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA) to address non-conformities.
• Collaborate with engineering and production departments to resolve product defects and improve product quality.
• Manage customer complaints and ensure timely and effective resolution.
• Train QA staff and production personnel on quality standards and procedures.
• Stay current with automotive industry quality regulations and best practices.

• Bachelor's degree in Engineering, Quality Management, or a related field.
• Minimum of 7 years of experience in quality assurance, with at least 3 years in a leadership role within the automotive industry.
• In-depth knowledge of automotive quality standards, such as IATF 16949 and APQP.
• Proven experience with quality control tools and methodologies (e.g., Six Sigma, Lean Manufacturing, SPC, FMEA, MSA).
• Experience in conducting internal and external audits.
• Strong analytical and problem-solving skills with a keen eye for detail.
• Excellent leadership, communication, and interpersonal skills.
• Proficiency in using quality management software and data analysis tools.
• Ability to work effectively in a fast-paced manufacturing environment.

• Competitive salary and performance-based bonuses.
• Comprehensive health insurance package.
• Opportunities for professional growth and certifications.
• Relocation assistance may be available.
• A challenging and rewarding role in a key automotive hub.
• Contribution to ensuring the highest product quality.

• Develop, implement, and maintain comprehensive quality assurance procedures and standards.
• Conduct regular inspections and audits of raw materials, in-process products, and finished goods.
• Analyze quality data, identify trends, and recommend corrective and preventive actions (CAPA).
• Collaborate with R&D and production teams to ensure new products meet stringent quality specifications.
• Investigate customer complaints related to product quality and implement solutions.
• Train production personnel on quality control procedures and best practices.
• Manage and maintain calibration records for all testing and measurement equipment.
• Stay abreast of industry quality standards, regulations, and emerging technologies.
• Prepare detailed quality reports for management review.
• Lead cross-functional teams in quality improvement projects.

• Bachelor's degree in Science, Engineering, Statistics, or a related discipline.
• Minimum of 5 years of hands-on experience in quality assurance or quality control within a manufacturing environment.
• In-depth knowledge of quality management systems (e.g., ISO 9001, Six Sigma, Lean Manufacturing).
• Proficiency in statistical analysis software and quality control tools.
• Experience with root cause analysis and implementing effective corrective actions.
• Excellent analytical and problem-solving abilities.
• Strong report-writing and presentation skills.
• Ability to interpret technical drawings and specifications.
• Detail-oriented with a commitment to accuracy.
• Familiarity with the manufacturing industry in **Abuja** is a plus.

• Competitive salary package.
• Health and wellness programs.
• Paid training and certification opportunities.
• Retirement savings plan.
• Generous annual leave.
• Collaborative and growth-oriented work environment.
• Exposure to cutting-edge manufacturing technologies.

Our client is seeking a meticulous and experienced Quality Assurance Specialist to ensure the highest standards of production in aviation manufacturing operations in **Gombe, Gombe, NG**. This role is critical for maintaining compliance with stringent aerospace quality regulations and ensuring the safety and reliability of manufactured components and systems. The QA Specialist will develop, implement, and manage quality control processes, conduct inspections, analyze production data, and drive continuous improvement initiatives. The ideal candidate possesses a strong understanding of quality management systems (QMS) within the aerospace industry, excellent analytical skills, and a keen eye for detail. You will collaborate closely with production, engineering, and supply chain teams to uphold our client's commitment to excellence. This position offers a blend of on-site quality oversight and the flexibility of hybrid work, based in **Gombe, Gombe, NG**. We are looking for individuals dedicated to upholding the rigorous standards expected in aviation manufacturing.

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with aerospace standards (e.g., AS9100).
• Conduct routine inspections and audits of manufacturing processes, materials, and finished products.
• Identify quality issues, non-conformities, and deviations, performing root cause analysis and implementing corrective actions.
• Develop and monitor quality control plans and procedures for manufacturing operations.
• Analyze production and quality data to identify trends, areas for improvement, and potential risks.
• Collaborate with engineering and production teams to resolve quality-related problems and implement process improvements.
• Ensure compliance with all relevant regulatory requirements and customer specifications.
• Manage documentation control, including standard operating procedures (SOPs), work instructions, and quality records.
• Train and mentor production staff on quality standards and procedures.
• Participate in supplier audits and evaluations to ensure the quality of incoming materials.

• Bachelor's degree in Engineering, Manufacturing Technology, or a related field, or equivalent experience.
• Minimum of 4 years of experience in Quality Assurance or Quality Control within the aerospace or manufacturing industry.
• In-depth knowledge of aerospace quality standards such as AS9100, ISO 9001.
• Proven experience with quality tools and methodologies, including root cause analysis (RCA), FMEA, SPC.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills, with the ability to document findings and communicate effectively.
• Proficiency in using quality management software and standard office applications.
• Ability to work independently and collaboratively within a team environment.
• Willingness to work a hybrid schedule, requiring regular on-site presence in **Gombe, Gombe, NG** for inspections and audits.
• Commitment to upholding the highest standards of quality and safety.

• Competitive salary package commensurate with experience and qualifications.
• Comprehensive health insurance coverage.
• Generous paid time off, including vacation, sick leave, and public holidays.
• Opportunities for professional development and certifications in quality management.
• Exposure to the intricacies of aviation manufacturing quality control.
• A dynamic work environment focused on continuous improvement and excellence.
• Retirement savings plan.
• Flexible hybrid work arrangement to support work-life balance.

Our client, a respected name in the pharmaceutical manufacturing industry, is seeking a diligent and experienced Quality Assurance Specialist to join their team in Sokoto, Sokoto, NG . This role is fundamental to ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements. The successful candidate will be responsible for implementing and maintaining robust quality management systems, conducting audits, and driving continuous improvement initiatives. This position offers an excellent opportunity to contribute to the safety and efficacy of medications, working within a team dedicated to upholding the highest levels of compliance. We are looking for an individual with a keen eye for detail and a strong understanding of pharmaceutical quality principles, who can operate effectively in a dynamic, hybrid work setting.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with regulatory standards (e.g., GMP, ISO).
• Conduct internal audits and participate in external audits by regulatory agencies and customers.
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Investigate deviations, customer complaints, and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPAs).
• Monitor and assess the performance of quality control processes.
• Ensure compliance with all applicable regulatory requirements, including those from NAFDAC and international bodies.
• Train personnel on quality procedures and GMP principles.
• Manage change control processes and risk assessments.
• Contribute to the continuous improvement of quality processes and systems.
• Maintain accurate and organized quality records.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
• Strong knowledge of Good Manufacturing Practices (GMP) and other relevant quality standards.
• Experience with auditing, CAPA management, and change control processes.
• Excellent analytical, problem-solving, and decision-making skills.
• Proficient in documentation and technical writing.
• Strong understanding of regulatory requirements for pharmaceuticals.
• Ability to work effectively both independently and as part of a team in a Hybrid work environment.
• Good communication and interpersonal skills.
• Must be legally authorized to work in Sokoto, Sokoto, NG .

Our client offers a competitive salary and benefits package that reflects your skills and experience. This includes health, dental, and vision insurance, along with retirement savings plans. We provide ample paid time off for rest and rejuvenation. Continuous professional development opportunities, including training programs and relevant certifications, are available. Our state-of-the-art facilities in Sokoto, Sokoto, NG offer a dynamic and engaging work environment. We foster a culture of quality and encourage innovation. Join us to build a rewarding career in pharmaceutical quality assurance.

Our client, a reputable pharmaceutical manufacturer, is seeking a detail-oriented Quality Assurance Specialist to join their operations in Uyo, Akwa Ibom . This role is crucial for upholding the highest standards of quality and compliance in pharmaceutical production. The QA Specialist will be responsible for reviewing and approving batch records, managing deviations and change controls, conducting internal audits, and ensuring adherence to Good Manufacturing Practices (GMP). The ideal candidate will have a strong understanding of pharmaceutical quality systems and a commitment to ensuring the safety and efficacy of manufactured products.

• Review and approve batch production and control records to ensure compliance with approved procedures and specifications.
• Manage deviations, investigations, and corrective and preventive actions (CAPAs) to identify root causes and implement effective solutions.
• Execute and manage change control procedures, assessing the impact of proposed changes on product quality.
• Conduct internal audits and participate in regulatory inspections to ensure ongoing compliance with GMP standards.
• Develop, implement, and maintain quality management system procedures and documentation.
• Provide training to personnel on GMP requirements, quality procedures, and relevant regulatory guidelines.
• Monitor key quality metrics and performance indicators, reporting findings to management.
• Participate in supplier qualification and auditing processes.
• Release finished product batches upon verification of compliance with all quality requirements.
• Support continuous improvement initiatives within the Quality Assurance department and manufacturing operations.
• Ensure all quality-related activities are meticulously documented and archived according to regulatory standards.

• Bachelor's degree in Pharmacy, Chemistry, Microbiology, or a related life science field.
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.
• Solid understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines (e.g., FDA, WHO).
• Experience with batch record review, deviation management, change control, and CAPA systems.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills.
• Ability to work effectively both independently and as part of a collaborative team.
• Proficiency in Microsoft Office Suite.
• Familiarity with Quality Management Systems (QMS) software is a plus.
• Knowledge of the pharmaceutical manufacturing processes is essential.
• Experience in the Uyo, Akwa Ibom area is advantageous.

Our client offers a competitive salary, comprehensive health insurance, paid time off, and opportunities for professional development and career advancement. This position is based in our facility in Uyo, Akwa Ibom , providing a stable and supportive work environment. Join a team dedicated to producing high-quality pharmaceuticals that improve patient lives. This is an excellent opportunity to grow your career in quality assurance within a respected pharmaceutical organization.

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with regulatory requirements.
• Conduct regular internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Manage and investigate deviations, CAPAs (Corrective and Preventive Actions), and change controls.
• Review and approve batch records, validation documents, and other quality-related documentation.
• Support external regulatory inspections and customer audits, preparing necessary documentation and responses.
• Participate in quality risk assessments and implement mitigation strategies.
• Train personnel on quality assurance procedures, GMP principles, and regulatory requirements.
• Monitor key quality metrics and prepare quality reports for management review.
• Contribute to the continuous improvement of quality processes and systems.
• Ensure all activities are conducted in compliance with local and international pharmaceutical regulations.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 5 years of experience in pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of Good Manufacturing Practices (GMP) and relevant regulatory guidelines (e.g., WHO, FDA, EMA).
• Proven experience in conducting audits, managing deviations, and implementing CAPAs.
• Strong understanding of pharmaceutical product development, manufacturing, and supply chain.
• Excellent analytical, problem-solving, and documentation skills.
• Strong interpersonal and communication skills, with the ability to influence effectively.
• Ability to work independently and manage multiple priorities in a deadline-driven environment.
• Proficiency in quality management software is a plus.