Quality Assurance Specialist

Placements24; Noord-Kaap; Hybrid; ZAR 500,000 - 700,000; Full time

Benefits offered by this job

Competitive salary

Health & retirement plans

Paid time off

Professional development

Remote-friendly with occasional travel

Job summary

Placements24 is seeking a proactive Quality Assurance Specialist to join our client’s pharmaceutical operations. The role is remote with occasional travel to Kimberley and other sites, focusing on ensuring GMP/ISO compliance and robust QA processes across manufacturing and product release.

You will audit, review batch records, manage QMS, and drive CAPA and risk mitigation while training staff and supporting continuous improvement in a flexible work setting.

Qualifications

• Bachelor's degree in a scientific or technical field.
• At least 3 years of QA experience in pharma or related industry.
• Solid knowledge of GMP, ISO standards, and regulatory requirements.
• Experience with deviation management, CAPA, and audit processes.
• Strong analytical and communication skills for remote work.

Responsibilities

• Participate in internal and external audits and inspections for GMP compliance.
• Review and approve batch records and validation protocols.
• Investigate deviations, non-conformances, and customer complaints; implement CAPAs.
• Assist in development and maintenance of the Quality Management System (QMS).
• Conduct risk assessments and implement mitigation strategies.
• Provide training on quality standards to relevant personnel.

Skills

Analytical thinking

Problem-solving

Communication skills

Remote collaboration

Education

Bachelor's degree in a scientific or technical field

Tools

QMS software

Job description

About the Role

Our client is seeking a proactive and experienced Quality Assurance Specialist to join their team, operating remotely with occasional travel. This role is crucial in ensuring that manufacturing processes and products consistently meet predefined quality standards and regulatory requirements. You will be involved in audits, inspections, quality system management, and continuous improvement initiatives within the pharmaceutical operations. This is an excellent opportunity for a QA professional looking to make a significant impact in a flexible work setting.

Key Responsibilities

• Participate in internal and external audits and inspections, ensuring compliance with GMP and other relevant regulations.
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Investigate deviations, non-conformances, and customer complaints, implementing corrective and preventative actions (CAPAs).
• Assist in the development and maintenance of the Quality Management System (QMS).
• Conduct risk assessments and implement mitigation strategies.
• Provide training on quality standards and procedures to relevant personnel.

Requirements

• Bachelor's degree in a scientific or technical field (e.g., Chemistry, Pharmacy, Engineering).
• Minimum of 3 years of experience in Quality Assurance within the pharmaceutical or related industry.
• Solid understanding of GMP, ISO standards, and regulatory requirements.
• Experience with deviation management, CAPA systems, and audit processes.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills for effective remote collaboration and occasional site visits.

Benefits

• Competitive annual salary and potential for bonuses.
• Comprehensive benefits package including health, dental, and retirement plans.
• Paid time off and holidays.
• Opportunities for professional development and continuing education.
• A flexible work environment with remote capabilities and occasional travel to Kimberley and other sites.