Pharmaceutical Quality Assurance Specialist

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

Benefits offered by this job

Competitive salary

Health insurance

Retirement benefits

Professional development opportunities

Paid time off

Job summary

Placements24 is seeking a diligent Pharmaceutical Quality Assurance Specialist in Benoni to strengthen our client’s quality management system. You will manage QMS processes, conduct audits, and lead deviation investigations to ensure products meet GMP and SAHPRA standards.

You will review batch records, validation protocols, and other critical documentation while providing training on QA principles, driving continual improvement and patient safety.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology or related science discipline.
• Minimum 4 years in Pharmaceutical Quality Assurance or QC role.
• Solid GMP and regulatory knowledge (SAHPRA).
• Experience with audits, deviation management, and CAPA systems.
• Strong analytical, problem-solving and documentation skills.
• Excellent interpersonal and communication skills.

Responsibilities

• Manage and maintain QMS including document control, change control, and record management.
• Conduct internal audits and participate in external audits by regulators and customers.
• Investigate deviations, non-conformances, and complaints; identify root causes and implement CAPAs.
• Review and approve batch records, validation protocols, and other quality docs.
• Ensure compliance with GMP and international standards; provide QA training.

Skills

GMP knowledge

QA audits

CAPA

Deviation management

Documentation

Analytical skills

Communication

Education

Bachelor's degree in Pharmacy, Chemistry, Biology

Tools

QMS software

Audit management tools

Job description

About the Role

Our client is seeking a diligent Pharmaceutical Quality Assurance Specialist to contribute to their robust quality management system in Benoni . This role is essential for ensuring that all pharmaceutical products meet stringent quality and regulatory standards throughout their lifecycle. You will be involved in various QA activities, including document control, audits, deviation management, and ensuring compliance with global regulatory requirements. This position offers a significant opportunity to impact product quality and patient safety within a company dedicated to excellence in pharmaceutical manufacturing and a culture that values integrity and continuous improvement.

Key Responsibilities

• Manage and maintain the company's quality management system (QMS), including document control, change control, and record management.
• Conduct internal audits and participate in external audits by regulatory authorities and customers.
• Investigate deviations, non-conformances, and customer complaints, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Ensure compliance with Good Manufacturing Practices (GMP) and relevant international regulatory standards.
• Provide training to personnel on quality assurance principles and procedures.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 4 years of experience in a Pharmaceutical Quality Assurance or Quality Control role.
• Solid understanding of GMP , regulatory requirements (e.g., SAHPRA), and quality systems.
• Experience with audit processes, deviation management, and CAPA systems.
• Strong analytical, problem-solving, and documentation skills.
• Excellent interpersonal and communication skills for effective collaboration.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health insurance and retirement benefits.
• Generous paid time off and opportunities for professional development.
• Exposure to various aspects of pharmaceutical quality assurance and regulatory compliance.
• A collaborative work environment committed to maintaining the highest quality standards.