Remote Pharma QA Specialist: GMP, CAPA & Compliance

Placements24; Mtubatuba Local Municipality; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Health insurance

Retirement savings plan

Flexible remote work schedule

Paid annual leave

Professional development support

Job summary

Placements24 seeks a diligent Remote Quality Assurance Specialist to ensure quality and regulatory compliance for pharmaceutical products, working remotely in the Richards Bay region. The role emphasizes robust quality systems and documentation integrity.

You will implement QMS, conduct audits, review batch records and CAPAs, and support GMP-compliant manufacturing while collaborating with multiple departments. Strong communication is essential.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology or related field.
• Minimum 4 years in Quality Assurance/Quality Control in pharma.
• In-depth GMP knowledge and familiarity with regulatory guidelines (FDA, SAHPRA).
• Experience with auditing, deviation management, CAPA and change control.
• Strong analytical, problem-solving and documentation skills.
• Excellent written and verbal communication.

Responsibilities

• Develop, implement and maintain QMS per regulatory standards.
• Conduct internal audits of processes, documentation and facilities.
• Review and approve batch records, validation protocols and QA docs.
• Investigate deviations and CAPAs to prevent recurrence.
• Provide QA oversight for manufacturing operations under GMP.
• Train staff on quality system requirements and compliance topics.

Skills

Quality Assurance

Regulatory compliance

Auditing

CAPA

GMP knowledge

Documentation

Education

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

Job description

Placements24 seeks a diligent Remote Quality Assurance Specialist to ensure quality and regulatory compliance for pharmaceutical products, working remotely in the Richards Bay region. The role emphasizes robust quality systems and documentation integrity.

You will implement QMS, conduct audits, review batch records and CAPAs, and support GMP-compliant manufacturing while collaborating with multiple departments. Strong communication is essential.