Quality Assurance (QA) Manager

Placements24

Cape Town

Hybrid

ZAR 1,000,000 - 1,500,000

Full time

3 days ago
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Benefits offered by this job

Hybrid work arrangement
Competitive executive salary
Comprehensive benefits package
Leadership development opportunities

Job summary

Placements24 in Kimberley seeks a seasoned QA Manager to lead the pharmaceutical quality systems, driving compliance with GMP, ISO, and global standards. You will establish and improve the QMS, oversee audits and CAPA, and champion documentation control across the organization.

The role demands a minimum of 8 years in QA within pharma with 3 years in management, plus strong leadership, communication, and decision-making abilities. A hybrid work setup supports flexibility and growth.

Qualifications

  • Minimum of 8 years of experience in QA within the pharmaceutical industry, with at least 3 years in a management role.
  • Extensive knowledge of GMP, ISO, and other relevant quality standards.
  • Proven experience in managing audits, inspections, and regulatory submissions.
  • Strong leadership, problem-solving, and decision-making skills.
  • Excellent communication and interpersonal abilities.

Responsibilities

  • Develop, implement, and maintain the QMS in GMP compliance.
  • Oversee internal and external audits, including follow-up actions.
  • Ensure all quality documentation like SOPs and batch records is up-to-date.
  • Lead CAPA system, investigate deviations and ensure effective resolutions.
  • Manage change control processes and assess/implement changes.
  • Provide training and guidance on QA principles and procedures.

Skills

Leadership
Audits & Inspections
CAPA management
GMP/ISO knowledge
Documentation control
Training & mentoring
Communication skills

Education

Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or related field
Advanced degree preferred

Job description

About the Role

Our client is seeking an experienced and results-oriented Quality Assurance (QA) Manager to lead their quality systems in Kimberley. This senior role is responsible for establishing, maintaining, and improving the overall quality management system to ensure compliance with global pharmaceutical standards and regulations. You will oversee all QA activities, including audits, inspections, document control, and CAPA management, fostering a culture of quality across the organization. This is a critical leadership position within a growing pharmaceutical company, offering the chance to make a significant impact on product quality and regulatory adherence in the Northern Cape.

Key Responsibilities
  • Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with GMP and other relevant regulations.
  • Oversee and manage internal and external audits, including preparation and follow-up actions.
  • Ensure all quality-related documentation, including SOPs, batch records, and validation protocols, are controlled and up-to-date.
  • Lead the Corrective and Preventive Actions (CAPA) system, investigating deviations and ensuring effective resolutions.
  • Manage change control processes and ensure that all changes are properly assessed and implemented.
  • Provide training and guidance to staff on quality assurance principles and procedures.
Requirements
  • Bachelor's degree in Pharmacy, Chemistry, Life Sciences, or a related field; advanced degree preferred.
  • Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a management role.
  • Extensive knowledge of GMP, ISO, and other relevant quality standards.
  • Proven experience in managing audits, inspections, and regulatory submissions.
  • Strong leadership, problem-solving, and decision-making skills.
  • Excellent communication and interpersonal abilities.
Benefits
  • Competitive executive salary and comprehensive benefits package.
  • Hybrid work arrangement providing flexibility and work-life integration.
  • Opportunity for significant professional growth and leadership development.
  • Be instrumental in ensuring the quality and safety of pharmaceutical products.
  • A dynamic and challenging work environment with a dedicated team.
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