Pharmaceutical Quality Assurance Specialist

Placements24; Soweto; Hybrid; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Hybrid work

Professional development

Job summary

Placements24 is seeking a detail-oriented Pharmaceutical Quality Assurance Specialist to enhance the quality management systems in Soweto. The role ensures compliance with GMP and internal policies, auditing, documenting, and implementing QC procedures to safeguard product integrity and patient safety.

The position is a hybrid role, collaborating across departments to foster a strong quality culture. The ideal candidate has deep GMP/QA knowledge, at least 4 years of pharmaceutical QA/QC

Qualifications

• Bachelor’s degree in Pharmacy, Science, Engineering, or a related field.
• Minimum of 4 years of experience in pharmaceutical QA or QC.
• In-depth knowledge of GMP and QA principles.
• Experience with QMS, audits, deviation investigations, and CAPA systems.
• Strong analytical skills and meticulous attention to detail.
• Excellent written and verbal communication abilities.

Responsibilities

• Develop, implement, and maintain the QMS in compliance with GMP.
• Conduct internal audits of processes, documentation, and facilities.
• Review and approve batch records, validation protocols, and change control docs.
• Investigate deviations, customer complaints, and non-conformances; implement CAPAs.
• Participate in regulatory inspections and audits by health authorities and customers.
• Train personnel on quality assurance procedures and GMP requirements.

Skills

GMP knowledge

QA/QC experience

Audit

CAPA

QMS

Regulatory compliance

Education

Bachelor's degree in Pharmacy or related field

Job description

About the Role

Our client is seeking a detail-oriented and experienced Pharmaceutical Quality Assurance Specialist to enhance their quality management systems in Soweto. This crucial role ensures that all pharmaceutical manufacturing processes and products adhere to stringent regulatory standards and internal quality policies. You will be responsible for auditing, documenting, and implementing quality control procedures to maintain the highest levels of product integrity and patient safety. Working in a hybrid capacity, you will collaborate with various departments to foster a strong quality culture throughout the organization. The ideal candidate possesses a deep understanding of GMP and QA principles within the pharmaceutical industry, dedicated to upholding excellence in every aspect of operations.

Key Responsibilities

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with GMP.


• Conduct internal audits of manufacturing processes, documentation, and facilities to ensure adherence to quality standards.


• Review and approve batch records, validation protocols, and change control documentation.


• Investigate deviations, customer complaints, and non-conformances, implementing corrective and preventive actions (CAPAs).


• Participate in regulatory inspections and audits by health authorities and customers.


• Train personnel on quality assurance procedures and GMP requirements.

Requirements

• Bachelor's degree in Pharmacy, Science, Engineering, or a related field.


• Minimum of 4 years of experience in pharmaceutical Quality Assurance or Quality Control.


• In-depth knowledge of Good Manufacturing Practices (GMP) and Quality Assurance principles.


• Experience with QMS, audits, deviation investigations, and CAPA systems.


• Strong analytical skills and meticulous attention to detail.


• Excellent written and verbal communication abilities.

Benefits

• Competitive annual salary with potential for performance bonuses.


• Comprehensive health, dental, and vision insurance coverage.


• Hybrid work arrangement offering a balance of office and remote work.


• Opportunities for professional development and certifications in quality assurance.


• A culture that prioritizes quality, safety, and continuous improvement.