Pharmaceutical Quality Assurance Specialist

Placements24; Welkom; On-site; ZAR 480,000 - 720,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Life insurance

Retirement fund

Continuous training & development

Relocation assistance

Job summary

Placements24 is seeking a detail-oriented Pharmaceutical Quality Assurance Specialist to join a Welkom manufacturing facility. The role ensures products meet quality, safety, and regulatory standards, implementing quality systems and leading audits.

You will investigate deviations, review batch records, and support CAPAs, with opportunities for professional development in a stable, growth-focused environment in the Free State region.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or related science.
• Minimum 3 years in QA within pharma or medical devices.
• Strong GMP knowledge and regulatory guidelines.
• Experience with CAPA, deviations, audits, and documentation.
• Proficient in quality management software and MS Office.

Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS) in line with GMP.
• Conduct internal audits of manufacturing processes and documentation for compliance.
• Investigate deviations and CAPAs; address customer complaints and non-conformances.
• Review and approve batch records, validation protocols, and change controls.
• Participate in external audits by regulators and customers.
• Provide training on quality assurance principles and SOPs.

Skills

QA expertise

GMP knowledge

Audit experience

CAPA implementation

Documentation control

Education

Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or related discipline

Tools

Quality management software

MS Office

Job description

About the Role

Our client is seeking a detail-oriented and proactive Pharmaceutical Quality Assurance Specialist to join their manufacturing facility in Welkom . This critical role ensures that all products manufactured meet the highest standards of quality, safety, and efficacy, adhering to strict regulatory requirements. You will be responsible for implementing and maintaining quality systems, conducting audits, and investigating deviations to uphold the integrity of our client's pharmaceutical operations. This is an excellent opportunity for a QA professional to make a significant impact in a key industrial hub within the Free State province.

Key Responsibilities

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with regulatory standards (e.g., GMP).
• Conduct internal audits of manufacturing processes, quality control procedures, and documentation to ensure compliance.
• Investigate deviations, non-conformances, and customer complaints, implementing corrective and preventive actions (CAPAs).
• Review and approve batch records, validation protocols, and change control documents.
• Participate in external audits conducted by regulatory agencies and customers.
• Provide training to personnel on quality assurance principles, GMP, and specific SOPs.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline.
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical or medical device industry.
• In-depth knowledge of Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Strong understanding of quality control processes, validation, and documentation practices.
• Excellent analytical, problem-solving, and critical thinking skills.
• Proficiency in using quality management software and standard office applications.

Benefits

• Competitive salary and annual bonus potential.
• Comprehensive medical aid, life insurance, and retirement fund.
• Opportunities for continuous professional development and specialized training.
• A stable and supportive work environment committed to excellence.
• Relocation assistance may be available for qualified candidates moving to Welkom .