Pharma QA Auditor: Hybrid Role with Site Visits & CAPA

Placements24; Bloemfontein; Hybrid; ZAR 360,000 - 520,000; Full time

Benefits offered by this job

Competitive salary

Health benefits

Professional development

Company vehicle for site visits

Hybrid work model

Generous leave

Job summary

Placements24 is seeking a meticulous Quality Assurance Auditor to join the quality management team in Bloemfontein. The role combines office-based tasks with on-site audits at various facilities to maintain GMP standards and regulatory compliance.

You will plan, conduct, and document audits, evaluate findings, and drive CAPA closures. A strong QA background in pharma and attention to detail are essential for success in this hybrid role.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology or related field.
• Proven experience in pharmaceutical Quality Assurance or Quality Control.
• In-depth knowledge of GMP principles and regulatory requirements for pharmaceuticals.
• Experience in conducting audits and managing audit programs.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills for reporting and interacting with auditees and authorities.

Responsibilities

• Plan, conduct, and document internal audits of manufacturing processes, quality systems, and documentation.
• Perform supplier audits to ensure compliance with quality agreements and regulatory standards.
• Evaluate audit findings, identify non-conformities, and recommend CAPAs.
• Follow up on CAPAs to ensure effective implementation and closure.
• Stay updated on GMP regulations and quality standards.
• Contribute to the continuous improvement of the Quality Management System.

Skills

Analytical skills

Problem-solving

Communication skills

Attention to detail

Auditing experience

Education

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

Job description

Placements24 is seeking a meticulous Quality Assurance Auditor to join the quality management team in Bloemfontein. The role combines office-based tasks with on-site audits at various facilities to maintain GMP standards and regulatory compliance.

You will plan, conduct, and document audits, evaluate findings, and drive CAPA closures. A strong QA background in pharma and attention to detail are essential for success in this hybrid role.