QA Specialist — GMP & Quality Compliance

Placements24; Queenstown; On-site; NZD 46,000 - 72,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Provident fund

Training & development

Job summary

Placements24 is seeking a detail-oriented Quality Assurance Specialist for a hands-on, on-site role in Queenstown (Eastern Cape). You will help maintain the QMS, perform internal audits, review batch records, SOPs, and validation protocols.

The ideal candidate holds a life science degree and 2–3 years of pharma QA/QC experience, with strong GMP knowledge, CAPA management, document control, and excellent communication. The role offers training and opportunities for professional growth.

Qualifications

• Bachelor's degree in a life science field (Pharmacy, Chemistry or Microbiology)
• 2–3 years' pharmaceutical QA/QC experience
• Strong GMP knowledge and regulatory familiarity
• Audits experience and CAPA management
• Excellent analytical and communication skills
• Proficient in document control and management
• Ability to work independently and as part of a team
• Meticulous attention to detail

Responsibilities

• Conduct internal quality audits and participate in external audits of suppliers and contract manufacturers.
• Review and approve quality-related documents, including batch records, SOPs, and validation protocols.
• Investigate deviations, OOS results, and customer complaints, implementing CAPAs as necessary.
• Monitor and ensure adherence to GMP and other applicable regulatory standards.
• Participate in change control activities and risk management processes.
• Maintain and update the QMS documentation.
• Train personnel on quality procedures and GMP principles.
• Support batch release activities by reviewing critical quality attributes.
• Stay informed about current regulatory requirements and industry best practices.

Education

Bachelor's degree in Pharmacy, Chemistry, Microbiology or related life science

Job description

Placements24 is seeking a detail-oriented Quality Assurance Specialist for a hands-on, on-site role in Queenstown (Eastern Cape). You will help maintain the QMS, perform internal audits, review batch records, SOPs, and validation protocols.

The ideal candidate holds a life science degree and 2–3 years of pharma QA/QC experience, with strong GMP knowledge, CAPA management, document control, and excellent communication. The role offers training and opportunities for professional growth.