Senior Pharmaceutical Quality Assurance Specialist

Placements24; Midrand; On-site; ZAR 900,000 - 1,200,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Retirement fund

Training opportunities

Modern facilities

Job summary

Placements24 is seeking an experienced Senior Pharmaceutical Quality Assurance Specialist to join a leading pharmaceutical company in Midrand. The role focuses on ensuring products meet GMP standards, maintaining QMS, and supporting regulatory compliance to safeguard patient safety and the company’s reputation.

You will audit across manufacturing, review batch records, CAPA, and mentor teams. The ideal candidate has a Bachelor’s in Life Sciences, strong GMP knowledge, 5+ years in QA, and

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology or related life science field.
• Master's degree is advantageous.
• Minimum 5 years of progressive experience in Quality Assurance in pharmaceutical or medical device industry.

Responsibilities

• Develop, implement and maintain QA policies across pharmaceutical manufacturing processes.
• Conduct internal GMP audits and ensure regulatory compliance.
• Review and approve batch records, validation protocols and change controls.
• Investigate deviations, non-conformances and customer complaints; implement CAPA.
• Provide training on quality standards, GMP and SOPs.
• Collaborate with regulatory bodies during inspections and audits.

Skills

Quality Assurance

GMP knowledge

Audit preparation

CAPA implementation

Analytical skills

Education

Bachelor's degree in Life Sciences

Master's degree advantageous

Job description

About the Role

Our client, a leading name in the pharmaceutical industry, is seeking an experienced and meticulous Senior Pharmaceutical Quality Assurance Specialist to join their dynamic team in Midrand . This pivotal role ensures that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements, contributing directly to patient safety and company reputation. You will be instrumental in maintaining and improving the quality management systems, working collaboratively with production, research, and regulatory affairs departments. This is an ideal opportunity for a detail-oriented professional passionate about quality and eager to make a significant impact within a reputable organization.

Key Responsibilities

• Develop, implement, and maintain quality assurance policies and procedures across all pharmaceutical manufacturing processes.
• Conduct regular internal audits to ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
• Review and approve batch records, validation protocols, and change control documents.
• Investigate deviations, non-conformances, and customer complaints, implementing corrective and preventive actions (CAPA).
• Provide training to personnel on quality standards, GMP, and relevant SOPs.
• Collaborate with external regulatory bodies during inspections and audits.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• A Master's degree is advantageous.
• Minimum of 5 years of progressive experience in Quality Assurance within the pharmaceutical or medical device industry.
• In-depth knowledge of GMP , regulatory requirements (e.g., SAHPRA), and quality management systems.
• Proven experience with audit preparation, deviation investigations, and CAPA implementation.
• Strong analytical, problem-solving, and decision-making skills.
• Excellent written and verbal communication skills in English.

Benefits

• Competitive annual salary and performance-based bonus opportunities.
• Comprehensive medical aid and retirement fund contributions.
• Opportunities for professional development and continuous training.
• A stimulating work environment with a focus on innovation and quality excellence.
• Access to state-of-the-art facilities and technology.