Quality Assurance Officer

Placements24; Bloemfontein; On-site; ZAR 420,000 - 540,000; Full time

Benefits offered by this job

Medical aid and provident fund

Professional development opportunities

On-site work environment

Paid time off

Job summary

Placements24 is seeking a detail-oriented Quality Assurance Officer to join their quality department in Bloemfontein. This on-site role focuses on maintaining the QMS, conducting audits, and ensuring GMP compliance to safeguard product integrity and patient safety.

Requirements include a science degree and at least 2 years in pharmaceutical QA/QC, with strong GMP knowledge and excellent attention to detail.

Qualifications

• Degree in Pharmacy, Chemistry, Microbiology or related scientific field.
• Minimum 2 years of pharma QA/QC experience.
• Strong GMP knowledge and quality systems.
• Experience with audits, deviations, and change controls.
• Attention to detail and analytical problem-solving.
• Effective communication and interpersonal skills.

Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS).
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Review and approve batch records, validation protocols, and change controls.
• Investigate deviations, CAPAs (Corrective and Preventive Actions), and customer complaints.
• Ensure GMP and regulatory compliance across operations.
• Train personnel on quality procedures and GMP requirements.

Skills

Attention to detail

Analytical problem-solving

Communication skills

Interpersonal skills

Education

Degree in Pharmacy, Chemistry, Microbiology or related field

Job description

About the Role

Our client is seeking a detail-oriented Quality Assurance Officer to join their established quality department in Bloemfontein . This on-site position is crucial for upholding the highest standards of quality and compliance across all manufacturing and operational processes. You will be responsible for implementing and maintaining the Quality Management System (QMS), conducting internal audits, and ensuring adherence to Good Manufacturing Practices (GMP). This role is vital for ensuring product integrity and patient safety within a structured, facility-based operational setting.

Key Responsibilities

• Develop, implement, and maintain the company's Quality Management System (QMS).
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Review and approve batch records, validation protocols, and change controls.
• Investigate deviations, CAPAs (Corrective and Preventive Actions), and customer complaints.
• Ensure all activities comply with GMP and relevant regulatory standards.
• Train personnel on quality procedures and GMP requirements.

Requirements

• Degree in Pharmacy, Chemistry, Microbiology, or a related scientific field.
• Minimum of 2 years of experience in pharmaceutical Quality Assurance or Quality Control.
• Strong understanding of Good Manufacturing Practices (GMP) and quality systems.
• Experience with audits, deviation management, and change control processes.
• Excellent attention to detail and analytical problem-solving skills.
• Effective communication and interpersonal abilities for an office environment.

Benefits

• Competitive salary and benefits package including medical aid and provident fund.
• Opportunities for professional development and training in quality management.
• Stable, on-site work environment within a reputable pharmaceutical company.
• Contribution to ensuring the quality and safety of pharmaceutical products.
• Paid time off and company-sponsored events.