3 Quality Assurance Specialist Pharmaceutical Manufacturing jobs in Placements24

Our client, a reputable pharmaceutical company, is looking for a diligent and detail-oriented Quality Assurance Specialist to join their operations in Zaria, Kaduna, NG . This role is essential for ensuring that all manufacturing processes and products adhere to the highest quality standards and regulatory requirements, including Good Manufacturing Practices (GMP). The successful candidate will be responsible for reviewing and approving batch records, participating in audits, managing deviations, and contributing to the continuous improvement of the quality management system. This is an excellent opportunity to build a career in pharmaceutical quality assurance within a well-established organization committed to patient safety and product integrity. The role is based full-time at our facility in Zaria, Kaduna, NG .

• Review and approve batch production and control records for accuracy and completeness.
• Investigate deviations, out-of-specification (OOS) results, and implement corrective and preventive actions (CAPAs).
• Participate in internal and external audits, ensuring readiness for regulatory inspections.
• Monitor and ensure compliance with cGMP regulations, company policies, and SOPs.
• Assist in the qualification and validation of equipment, processes, and analytical methods.
• Manage change control processes, assessing the impact of proposed changes on product quality.
• Conduct quality risk assessments and contribute to quality by design initiatives.
• Train personnel on quality systems and GMP compliance.
• 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.
• Solid understanding of cGMP regulations and quality management systems.
• Experience with batch record review, deviation management, and CAPA systems.
• Familiarity with audit processes and regulatory inspections.
• Strong analytical and problem-solving skills with excellent attention to detail.
• Effective communication, both written and verbal, with the ability to document findings clearly.
• Proficiency in Microsoft Office Suite and common quality management software.
• Ability to work effectively both independently and as part of a team.
• Must be available for full-time, on-site work in Zaria, Kaduna, NG .

Our client provides a competitive annual salary, commensurate with experience. Employees enjoy comprehensive health insurance coverage, including medical and dental plans. A retirement savings plan is available with employer contributions. Opportunities for professional growth are supported through ongoing training and development programs. Paid time off includes annual leave, sick leave, and observance of public holidays. This position in Zaria, Kaduna, NG offers a stable and supportive work environment where quality and patient safety are paramount. Join a team dedicated to upholding the highest standards in pharmaceutical manufacturing.

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.