Quality Assurance Manager - Pharmaceutical Manufacturing

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

Benefits offered by this job

Competitive salary

Health, life & disability insurance

Retirement plan

Generous leave & paid sick leave

Career development

Job summary

Placements24 partners with a pharmaceutical manufacturer in Pretoria to recruit a seasoned Quality Assurance Manager. You will establish and maintain a robust QMS ensuring compliance with GMP, ISO standards and SAHPRA regulatory requirements across the site.

Lead QA/QC activities, audits, CAPA, change control, and deviation investigations while mentoring staff and fostering a strong quality culture to safeguard product integrity and patient safety.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Engineering, or related field.
• 6+ years QA experience in pharmaceutical manufacturing.
• At least 3 years in a management role.
• Strong GMP, ISO knowledge and regulatory familiarity (SAHPRA).

Responsibilities

• Develop, implement, and manage the QMS.
• Oversee QA/QC activities in manufacturing facility.
• Lead internal audits and coordinate external inspections.
• Drive deviation investigations, CAPA, and change control.
• Mentor QA/QC staff and promote quality culture.

Skills

QA Leadership

GMP Knowledge

Audits

CAPA

Change Control

Regulatory Compliance

Education

Bachelor's degree (Pharma/Chem/Eng)

Job description

About the Role

Our client is looking for a seasoned and proactive Quality Assurance Manager to lead their quality operations in Pretoria. You will be responsible for establishing and maintaining a robust quality management system that ensures compliance with all relevant pharmaceutical manufacturing standards and regulatory requirements. This leadership position is crucial for upholding the integrity and safety of our client's products, ensuring excellence in every aspect of their operations.

Key Responsibilities

• Develop, implement, and manage the company's Quality Management System (QMS).
• Oversee all quality control and quality assurance activities within the manufacturing facility.
• Conduct internal audits and host external regulatory inspections and customer audits.
• Manage deviation investigations, CAPA implementation, and change control processes.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant industry standards.
• Train and mentor QA/QC staff, fostering a strong quality culture throughout the organization.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Engineering, or a related field.
• Minimum of 6 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 regulatory requirements (e.g., SAHPRA).
• Proven experience in developing and maintaining QMS, conducting audits, and managing regulatory inspections.
• Strong leadership, decision-making, and problem-solving abilities.
• Excellent written and verbal communication skills.

Benefits

• Highly competitive salary package with annual performance reviews and bonuses.
• Comprehensive health, life, and disability insurance coverage.
• Retirement savings plan with employer contributions.
• Generous annual leave and paid sick leave policy.
• Opportunities for career advancement and leadership development within a growing company.