Quality Assurance Auditor

Placements24; Klerksdorp; Hybrid; ZAR 420,000 - 600,000; Full time

Benefits offered by this job

Health insurance

Hybrid work model

Professional development and auditing‑

Retirement plan

Job summary

Placements24 is seeking a Quality Assurance Auditor in Klerksdorp to conduct internal and external GMP/GDP audits, including on-site inspections and remote assessments. You will review SOPs, CAPAs, and supplier quality systems while traveling as needed.

The ideal candidate holds a Bachelor’s degree in a science field and 3–5 years of QA or auditing experience, with strong analytical and reporting skills and the ability to work in a hybrid environment.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology or related field required.
• Minimum 3–5 years in Pharmaceutical Quality Assurance or Auditing.
• In-depth knowledge of GMP and GDP regulations and guidelines.
• Experience conducting audits and assessing quality systems.
• Strong analytical, problem‑solving, and report writing skills.
• Willingness to travel for on-site audits and operate in a hybrid setup.

Responsibilities

• Plan, conduct, and report on internal and external audits of manufacturing sites, suppliers, and distribution channels.
• Evaluate compliance with GMP, GDP, and other applicable quality regulations and standards.
• Identify non-compliance issues, assess impact, and recommend CAPAs.
• Follow up on CAPA implementation and effectiveness.
• Review and approve quality documentation, including SOPs and validation protocols.
• Provide training and guidance on quality systems and compliance requirements.

Skills

Auditing

Analytical skills

Report writing

Travel readiness

Quality systems

Education

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

Job description

About the Role

Our client is seeking a diligent and experienced Quality Assurance Auditor to join their team in Klerksdorp . This crucial role involves conducting internal and external audits to ensure compliance with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant quality standards within the pharmaceutical industry. You will be instrumental in maintaining the high standards of quality and integrity of our client's products and processes. This hybrid role combines remote auditing capabilities with essential on-site inspections, offering a flexible yet impactful career opportunity. We are looking for a professional with a sharp eye for detail and a strong commitment to quality.

Key Responsibilities

• Plan, conduct, and report on internal and external audits of manufacturing sites, suppliers, and distribution channels.
• Evaluate compliance with GMP , GDP, and other applicable quality regulations and standards.
• Identify non-compliance issues, assess their impact, and recommend corrective and preventative actions (CAPAs).
• Follow up on the implementation and effectiveness of CAPAs.
• Review and approve quality-related documentation, including SOPs and validation protocols.
• Provide training and guidance to internal staff and suppliers on quality systems and compliance requirements.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3-5 years of experience in Pharmaceutical Quality Assurance or Auditing.
• In-depth knowledge of GMP and GDP regulations and guidelines.
• Experience in conducting audits and assessing quality systems.
• Strong analytical, problem-solving, and report-writing skills.
• Ability to travel for on-site audits and work effectively in a hybrid setup.

Benefits

• Competitive salary and annual performance review.
• Comprehensive health, dental, and vision insurance.
• Retirement fund contribution.
• Opportunities for professional development and certification in quality auditing.
• A collaborative environment focused on ensuring the highest standards of pharmaceutical quality.