Quality Assurance Manager - Pharmaceuticals

Placements24; Klerksdorp; On-site; ZAR 900,000 - 1,500,000; Full time

Benefits offered by this job

Competitive salary

Health, dental, vision insurance

Paid time off

Retirement plan with employer match

Professional development

Job summary

Placements24 seeks a seasoned Quality Assurance Manager to lead QA operations at a pharmaceutical manufacturing facility in Klerksdorp. You will oversee the QMS, ensure GMP/ISO compliance, manage audits and inspections, and drive continuous product quality improvements in a hands-on environment.

The role requires strong leadership, deep QA knowledge, and a track record of implementing CAPA and change control in a regulated setting.

Qualifications

• Bachelor's degree in a scientific field (Pharmacy, Chemistry, Biology or related).
• Minimum 8 years in Quality Assurance in pharma, with at least 3 years in management.
• Deep knowledge of GMP, ISO standards and pharmaceutical regulations.

Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS).
• Ensure compliance with GMP, ISO and regulatory requirements.
• Oversee audits, regulatory inspections, and CAPA/change control actions.
• Lead the QA team with guidance, training and performance management.
• Review and approve batch records, validation protocols and change controls.
• Investigate deviations, complaints and recalls; implement preventive measures.

Skills

Leadership

Communication

Problem-solving

Working under pressure

Education

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

Tools

QMS software

CAPA system

Change control process

Job description

About the Role

Our client is seeking a seasoned Quality Assurance Manager to lead their quality operations within the pharmaceutical manufacturing facility in Klerksdorp . This critical role involves overseeing all aspects of the quality management system, ensuring adherence to stringent regulatory standards and driving continuous improvement in product quality and safety. You will be responsible for maintaining compliance with GMP (Good Manufacturing Practices) and other relevant pharmaceutical regulations. The ideal candidate will possess strong leadership skills, a deep understanding of pharmaceutical quality systems, and a commitment to upholding the highest standards in a hands-on operational environment.

Key Responsibilities

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


• Ensure compliance with all relevant regulatory requirements, including GMP, FDA, and other health authority standards.


• Oversee internal and external audits, manage regulatory inspections, and implement corrective actions.


• Lead the QA team, providing guidance, training, and performance management.


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


• Investigate deviations, customer complaints, and product recalls, implementing preventative measures.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.


• Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a management role.


• In-depth knowledge of GMP, ISO standards, and pharmaceutical regulatory requirements.


• Proven experience with quality systems, audits, CAPA, and change control.


• Strong leadership, communication, and problem-solving abilities.


• Ability to work effectively under pressure and meet strict deadlines.

Benefits

• Highly competitive salary and comprehensive bonus structure.


• Extensive health, dental, and vision insurance coverage.


• Generous paid time off and holiday schedule.


• Retirement savings plan with employer match.


• Opportunities for professional development and advanced training.


• A stable and rewarding work environment focused on excellence.