Quality Assurance Specialist - Pharmaceutical Manufacturing

Placements24; Centurion; Hybrid; ZAR 350,000 - 550,000; Full time

Benefits offered by this job

Health benefits

Retirement plan

Training & development opportunities

Career growth potential

Job summary

Placements24 is seeking a detail-oriented Quality Assurance Specialist in Centurion, Gauteng. The role focuses on implementing and maintaining QMS, conducting internal audits, reviewing batch records, and managing CAPAs to ensure GMP-compliant operations.

The successful candidate will collaborate with production, R&D, and other departments, train personnel on quality procedures, and monitor quality metrics to drive continuous improvement in a fast-paced pharmaceutical setting.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in a Quality Assurance or Quality Control role within the pharmaceutical industry.
• In-depth knowledge of Good Manufacturing Practices (GMP) and other relevant quality regulations.
• Experience with quality systems, documentation control, audits, and CAPA management.
• Strong analytical and problem-solving skills, with meticulous attention to detail.
• Excellent written and verbal communication skills.
• Ability to work independently and as part of a team.
• Proficiency in Microsoft Office Suite and experience with quality management software is a plus.
• Must be located in or willing to relocate to Centurion, Gauteng.

Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with relevant regulatory standards (e.g., GMP, ISO).
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Review and approve batch records, deviation reports, and change control requests.
• Investigate quality complaints and non-conformances, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Participate in external audits and inspections by regulatory authorities and customers.
• Ensure that all personnel are trained on quality procedures and regulatory requirements.
• Monitor key quality metrics and provide regular reports to management.
• Collaborate with production, R&D, and other departments to resolve quality issues and implement improvements.
• Maintain all quality-related documentation in a systematic and accessible manner.

Skills

Quality Assurance

Quality Control

Audits

CAPA management

Regulatory compliance

Analytical skills

Detail-oriented

Independent work

Education

Bachelor's degree in Pharmacy

Bachelor's degree in Chemistry

Bachelor's degree in Biology

Related scientific field

Tools

MS Office

Quality management software

Job description

About the Role

Our client, a respected pharmaceutical manufacturer located in Centurion, Gauteng, is looking for a detail-oriented Quality Assurance Specialist. This role is instrumental in upholding the highest standards of quality and compliance throughout the pharmaceutical manufacturing process. The QA Specialist will be responsible for implementing and maintaining quality management systems, conducting internal audits, and ensuring all operations meet stringent regulatory requirements. This is an exciting opportunity to contribute to the production of safe and effective medicines within a company that prioritizes quality and innovation. You will be part of a dedicated team focused on ensuring product integrity and patient safety. We encourage a proactive approach to quality enhancement and continuous improvement.

Key Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with relevant regulatory standards (e.g., GMP, ISO).
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Review and approve batch records, deviation reports, and change control requests.
• Investigate quality complaints and non-conformances, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Participate in external audits and inspections by regulatory authorities and customers.
• Ensure that all personnel are trained on quality procedures and regulatory requirements.
• Monitor key quality metrics and provide regular reports to management.
• Collaborate with production, R&D, and other departments to resolve quality issues and implement improvements.
• Maintain all quality-related documentation in a systematic and accessible manner.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in a Quality Assurance or Quality Control role within the pharmaceutical industry.
• In-depth knowledge of Good Manufacturing Practices (GMP) and other relevant quality regulations.
• Experience with quality systems, documentation control, audits, and CAPA management.
• Strong analytical and problem-solving skills, with meticulous attention to detail.
• Excellent written and verbal communication skills.
• Ability to work independently and as part of a team.
• Proficiency in Microsoft Office Suite and experience with quality management software is a plus.
• Must be located in or willing to relocate to Centurion, Gauteng.

Benefits

• Competitive annual salary.
• Comprehensive health, dental, and vision benefits package.
• Retirement savings plan.
• Paid sick leave and vacation days.
• Opportunities for professional development and training.
• A stable and supportive work environment.
• Employee wellness programs.
• Potential for career growth within the organization.