Pharma QA Specialist – Hybrid Role, QMS & GMP Excellence

Placements24; LegKraal Gate; Híbrido; ZAR 420.000 - 560.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid role

Medical aid

Retirement benefits

Professional development

Quality team

Career progression

Descripción de la vacante

Placements24 in Mahikeng, North West, seeks a Pharmaceutical Quality Assurance Specialist to uphold GMP and QMS across operations. You will develop, implement, and audit quality processes to ensure product safety and regulatory compliance.

With 3–5 years of QA experience, you will lead internal audits, CAPA management, and training, collaborating with multiple teams to continually improve quality metrics and maintain industry standards.

Formación

• Bachelor's degree in a related field (Pharmacy, Chemistry, Life Sciences)
• 3–5 years of QA experience in the pharmaceutical industry
• Strong GMP, ICH knowledge and regulatory requirements
• Experience conducting internal audits and managing CAPA
• Excellent analytical, detail-oriented, and documentation skills
• Strong communication and ability to work both independently and in a team

Responsabilidades

• Develop, implement, and maintain the QMS.
• Conduct internal audits of manufacturing processes and documents.
• Review and approve batch records and change controls.
• Investigate deviations and CAPAs; implement effective solutions.
• Participate in external regulatory inspections and audits.
• Provide training on quality standards and GMP.
• Monitor quality metrics and report performance improvements.
• Ensure products meet quality specifications.

Conocimientos

GMP Knowledge

ICH Guidelines

Internal Audits

CAPA Management

Quality Documentation

Analytical Skills

Educación

Bachelor's degree in Pharmacy or related field

Herramientas

QMS software

Audit Tools

Descripción del empleo

Placements24 in Mahikeng, North West, seeks a Pharmaceutical Quality Assurance Specialist to uphold GMP and QMS across operations. You will develop, implement, and audit quality processes to ensure product safety and regulatory compliance.

With 3–5 years of QA experience, you will lead internal audits, CAPA management, and training, collaborating with multiple teams to continually improve quality metrics and maintain industry standards.