Quality Assurance Specialist - Pharmaceuticals

Placements24; Mtubatuba Local Municipality; On-site; ZAR 420,000 - 540,000; Full time

Benefits offered by this job

Competitive salary

Medical & retirement benefits

Professional development and training

Stable work environment

Impact on patient safety

Job summary

Placements24 is seeking a diligent Quality Assurance Specialist in Richards Bay, KwaZulu-Natal. You will develop, implement, and maintain QMS, conduct audits, and investigate deviations to ensure pharmaceutical products meet quality and regulatory standards.

The role requires a Bachelor’s degree in a related field and at least 3 years in QA/QC within pharma, with strong GMP knowledge and communication skills for thorough documentation and reporting.

Qualifications

• Bachelor's degree required in a scientific field (Pharmacy, Chemistry, Biology, or similar).
• Minimum 3 years' QA/QC experience in pharma.
• Strong GMP knowledge and regulatory familiarity.
• Experience with audits, deviations, and CAPA systems.
• Excellent written and verbal communication for Richards Bay documentation.

Responsibilities

• Implement and maintain QMS (GMP-aligned).
• Conduct internal audits of manufacturing processes and facilities.
• Investigate quality complaints, deviations, and CAPAs.
• Review and approve batch records, validation protocols, and docs.
• Collaborate with production, R&D, and regulatory teams to resolve issues.
• Stay updated on regulatory guidelines and best practices.

Skills

GMP knowledge

Quality audits

CAPA investigations

Analytical thinking

Documentation skills

Education

Bachelor's degree in Pharmacy, Chemistry, Biology, or related field

Job description

About the Role

Our client seeks a diligent and detail-oriented Quality Assurance Specialist to join their team in Richards Bay, KwaZulu-Natal . This role is essential for ensuring that all pharmaceutical products manufactured and distributed meet stringent quality standards and regulatory compliance requirements. You will be responsible for developing, implementing, and maintaining quality management systems, conducting audits, and investigating deviations to uphold the integrity of our client's products and processes. The ideal candidate will have a strong background in quality control and assurance within the pharmaceutical industry, demonstrating a commitment to excellence and patient safety.

Key Responsibilities

• Implement and maintain the company's Quality Management System (QMS) in accordance with regulatory standards (e.g., GMP).
• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure compliance.
• Investigate product quality complaints, deviations, and non-conformances, implementing corrective and preventive actions (CAPAs).
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Collaborate with production, R&D, and regulatory affairs teams to resolve quality issues.
• Stay updated on relevant regulatory guidelines and industry best practices for pharmaceutical quality.

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.
• Thorough understanding of Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Experience with quality audits, deviation investigations, and CAPA systems.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills, particularly for documentation and reporting in Richards Bay.

Benefits

• Competitive salary commensurate with experience.
• Comprehensive medical and retirement benefits.
• Opportunities for professional development and training in pharmaceutical quality systems.
• A stable and supportive work environment focused on high-quality production.
• Contribution to ensuring the safety and efficacy of pharmaceutical products in KwaZulu-Natal.