Pharmaceutical Quality Assurance Specialist

Placements24; LegKraal Gate; Hybrid; ZAR 420,000 - 560,000; Full time

Benefits offered by this job

Hybrid role

Medical aid

Retirement benefits

Professional development

Quality team

Career progression

Job summary

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.

Qualifications

• 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

Responsibilities

• 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.

Skills

GMP Knowledge

ICH Guidelines

Internal Audits

CAPA Management

Quality Documentation

Analytical Skills

Education

Bachelor's degree in Pharmacy or related field

Tools

QMS software

Audit Tools

Job description

About the Role Our client, a reputable pharmaceutical company, is seeking a diligent and experienced Pharmaceutical Quality Assurance Specialist to join their team in Mahikeng, North West. This role is integral to maintaining the company’s high standards of quality and compliance across all pharmaceutical operations. You will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), conducting internal audits, and ensuring adherence to GMP and other relevant regulatory guidelines. The ideal candidate will possess a thorough understanding of quality assurance principles in the pharmaceutical industry and a keen eye for detail. This position offers a challenging yet rewarding career in ensuring the safety and efficacy of pharmaceutical products. You will collaborate with various departments to uphold quality standards throughout the product lifecycle.

Key Responsibilities

• Develop, implement, and maintain the company's Quality Management System (QMS).
• Conduct internal audits of manufacturing processes, documentation, and systems to ensure compliance with GMP and regulatory standards.
• Review and approve batch records, validation documents, and change controls.
• Investigate deviations, CAPAs (Corrective and Preventive Actions), and customer complaints, implementing effective solutions.
• Participate in external regulatory inspections and customer audits.
• Provide training to personnel on quality standards and GMP requirements.
• Monitor and analyze quality metrics, reporting on performance and identifying areas for improvement.
• Ensure that all pharmaceutical products meet established quality specifications.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or a related field.
• Minimum of 3-5 years of experience in Quality Assurance within the pharmaceutical industry.
• Strong knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
• Proven experience in conducting internal audits and managing CAPA systems.
• Excellent analytical and problem-solving skills.
• Strong attention to detail and accuracy in documentation and data review.
• Good written and verbal communication skills.
• Ability to work independently and collaboratively within a team environment.

Benefits

• Competitive salary.
• Comprehensive medical aid.
• Retirement fund benefits.
• Hybrid role providing a structured work environment with opportunities for both in-office collaboration and remote flexibility, based in Mahikeng, North West.
• Continuous learning and professional development opportunities, including training on new quality standards and regulatory updates.
• Dedicates quality team focused on upholding the highest standards in the pharmaceutical industry.
• Clear career progression path.