Pharmaceutical Quality Assurance Specialist

Placements24; Klerksdorp; Hybrid; ZAR 480,000 - 720,000; Full time

Benefits offered by this job

Competitive salary

Medical, dental & vision insurance

Generous paid time off

Professional development opportunities

Supportive QA environment

Job summary

Placements24 is seeking a meticulous Pharmaceutical Quality Assurance Specialist to join their team in Klerksdorp. This role focuses on maintaining high quality across pharmaceutical operations, ensuring regulatory compliance and policy alignment.

You will review documentation, participate in audits, investigate deviations, implement CAPAs, and contribute to continuous quality system improvements, while training staff on GMP and related topics.

Qualifications

• Bachelor’s degree in Pharmacy, Chemistry, Biology, or related field.
• Minimum 3 years’ experience in pharmaceutical QA or QC.
• Solid GMP/ICH knowledge and regulatory understanding.
• Experience with document control, change control, deviation management, and CAPA systems.
• Strong analytical and communication skills.

Responsibilities

• Review and approve batch records, validation reports, and quality documents.
• Participate in audits and ensure GMP compliance.
• Investigate deviations, non-conformances, and CAPA implementation.
• Develop and maintain quality management system procedures and SOPs.
• Prepare quality metrics reports for management review.
• Provide training on GMP and compliance topics.

Skills

Analytical skills

Problem solving

Attention to detail

Written communication

Verbal communication

Education

Bachelor’s degree in Pharmacy/Chemistry/Biology

Job description

About the Role

Our client is seeking a meticulous and knowledgeable Pharmaceutical Quality Assurance Specialist to join their team in Klerksdorp . This role is integral to maintaining the highest standards of quality across all pharmaceutical operations, ensuring compliance with regulatory requirements and company policies. You will be involved in reviewing documentation, auditing processes, and contributing to the continuous improvement of quality systems. This position offers a challenging and rewarding career path within the highly regulated pharmaceutical sector, ensuring the safety and efficacy of medicinal products.

Key Responsibilities

• Review and approve batch records, validation reports, and other quality-related documentation.
• Participate in internal and external audits, ensuring compliance with GMP and other relevant regulations.
• Investigate deviations, non-conformances, and customer complaints, implementing corrective and preventive actions (CAPAs).
• Develop, implement, and maintain quality management system procedures and SOPs.
• Monitor key quality indicators and prepare reports for management review.
• Provide training to personnel on quality systems, GMP, and other relevant compliance topics.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 3 years of experience in pharmaceutical Quality Assurance or Quality Control.
• Solid understanding of GMP, ICH guidelines, and regulatory requirements for pharmaceutical manufacturing.
• Experience with document control, change control, deviation management, and CAPA systems.
• Strong analytical and problem-solving skills, with excellent attention to detail.
• Effective written and verbal communication skills, with the ability to present information clearly.

Benefits

• Competitive salary commensurate with experience.
• Comprehensive health, dental, and vision insurance coverage.
• Generous paid time off and company holidays.
• Opportunities for professional development and career advancement in QA.
• A supportive and collaborative work environment fostering quality and compliance.