GMP Quality Assurance Specialist — Hybrid, Growth & Training

Placements24; Kempton Park; Hybrid; ZAR 480,000 - 720,000; Full time

Benefits offered by this job

Hybrid work model

Comprehensive medical, dental, and vis

Bonuses potential

Professional growth opportunities

Training programs and workshops

Job summary

Placements24 is seeking a meticulous Pharmaceutical Quality Assurance Specialist to join their team in Tembisa. This hybrid role focuses on maintaining high standards of quality and compliance across manufacturing processes, developing robust quality systems, and ensuring regulatory adherence.

The position emphasizes collaboration with production, R&D, and regulatory affairs, handling audits, CAPAs, and batch documentation to safeguard product quality and patient safety.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology, or related field.
• 3–5 years' experience in QA or QC in the pharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines and quality systems.
• Experience with documentation review, audit procedures, and CAPA management.
• Strong analytical and problem-solving skills with excellent communication.

Responsibilities

• Develop and implement QA policies, procedures, and systems to ensure GMP compliance.
• Conduct internal audits and inspections of manufacturing processes, facilities, and documentation.
• Review and approve batch records, validation protocols, and change control documents.
• Investigate deviations, customer complaints, and OOS results; implement CAPAs.
• Collaborate with production, R&D, and regulatory affairs to ensure product quality.
• Participate in external audits by regulatory authorities and customers.

Skills

Quality Assurance

GMP knowledge

Auditing

CAPA management

Analytical skills

Communication

Education

Bachelor's degree in Pharmacy, Chemistry, Biology, or related field

Job description

Placements24 is seeking a meticulous Pharmaceutical Quality Assurance Specialist to join their team in Tembisa. This hybrid role focuses on maintaining high standards of quality and compliance across manufacturing processes, developing robust quality systems, and ensuring regulatory adherence.

The position emphasizes collaboration with production, R&D, and regulatory affairs, handling audits, CAPAs, and batch documentation to safeguard product quality and patient safety.