Pharmaceutical Quality Assurance Officer

Placements24; Mossel Bay; On-site; ZAR 420,000 - 660,000; Full time

Benefits offered by this job

Competitive salary

Annual bonuses

Medical benefits

Retirement benefits

Professional development

Paid time off

Job summary

Placements24 in Mossel Bay is seeking a meticulous Pharmaceutical Quality Assurance Officer to ensure all pharmaceutical products meet stringent quality standards and regulatory requirements. You will develop, implement, and maintain the company's Quality Management System (QMS) and support continuous improvement.

The ideal candidate holds a Bachelor's degree in Pharmacy, Chemistry, or Microbiology, with 4+ years in pharmaceutical QA, deep GMP knowledge, auditing experience, and strong

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Microbiology, or related scientific discipline.
• Minimum of 4 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, regulatory affairs, and quality control principles.
• Experience with auditing, document control, and risk management.
• Strong analytical and problem-solving skills, with excellent attention to detail.

Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with regulatory standards.
• Conduct internal audits and participate in external audits by regulatory agencies and customers.
• Review and approve batch records, manufacturing documentation, and validation reports.
• Manage and investigate deviations, CAPAs (Corrective and Preventive Actions), and change controls.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant pharmaceutical regulations.

Job description

About the Role

Our client, a respected entity in the pharmaceutical manufacturing sector, is looking for a meticulous Pharmaceutical Quality Assurance Officer to join their dedicated team in Mossel Bay . This role is essential for ensuring that all pharmaceutical products meet rigorous quality standards and comply with national and international regulatory requirements. You will play a key role in developing, implementing, and maintaining the company's Quality Management System (QMS). The ideal candidate is process-oriented, committed to excellence, and possesses a strong understanding of GMP principles.

Key Responsibilities

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with regulatory standards.
• Conduct internal audits and participate in external audits by regulatory agencies and customers.
• Review and approve batch records, manufacturing documentation, and validation reports.
• Manage and investigate deviations, CAPAs (Corrective and Preventive Actions), and change controls.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant pharmaceutical regulations .

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Microbiology, or a related scientific discipline.
• Minimum of 4 years of experience in Quality Assurance within the pharmaceutical industry.
• In-depth knowledge of GMP, regulatory affairs, and quality control principles.
• Experience with auditing, document control, and risk management.
• Strong analytical and problem-solving skills, with excellent attention to detail.

Benefits

• Competitive salary and potential for annual bonuses.
• Comprehensive medical and retirement benefits package.
• Opportunities for professional development and advanced training in quality management.
• A stable and supportive work environment within a growing company.
• Generous paid time off and wellness initiatives.