Senior Analytical Chemist - Pharmaceutical QC

Placements24; Stellenbosch; Hybrid; ZAR 700,000 - 900,000; Full time

Benefits offered by this job

Competitive salary

Professional development

Exposure to advanced analytics

Structured GMP environment

Team collaboration

Patient safety impact

Job summary

Placements24 client seeks an experienced Senior Analytical Chemist to strengthen the Quality Control team at a pharmaceutical site in Stellenbosch. You will lead method development, validation, and routine analysis to ensure product quality and regulatory compliance.

Responsibilities include developing/validating methods (HPLC, GC, UV-Vis, FTIR, dissolution), troubleshooting OOS, implementing CAPAs, maintaining GMP-compliant lab practices, and mentoring junior staff.

Qualifications

• MSc or PhD in Chemistry or Analytical Chemistry.
• Minimum 5 years in pharmaceutical QC or analytical development.
• Extensive experience with HPLC, GC, and wet chemistry.
• Thorough understanding of GMP, ICH, and regulatory requirements.

Responsibilities

• Develop, validate, and implement analytical methods for raw materials and finished products.
• Perform routine testing using HPLC, GC, UV-Vis, FTIR, and dissolution.
• Investigate OOS results and implement CAPAs.
• Maintain lab equipment and ensure calibration per GMP.
• Review and approve analytical data and reports.
• Mentor and train junior analytical chemists and technicians.

Skills

Analytical skills

Attention to detail

Problem solving

Education

MSc or PhD in Chemistry

Tools

HPLC

GC

UV-Vis

FTIR

Dissolution testing

Job description

Our client is seeking an experienced Senior Analytical Chemist to strengthen their Quality Control department at their pharmaceutical manufacturing site in Stellenbosch . This critical role involves ensuring the quality and compliance of raw materials, intermediates, and finished products through rigorous analytical testing. You will be responsible for method development, validation, and routine analysis, playing a key part in maintaining the highest standards of pharmaceutical quality and regulatory adherence within a demanding yet rewarding sector.

Key Responsibilities

• Develop, validate, and implement analytical methods for raw materials, in-process samples, and finished pharmaceutical products.
• Perform routine testing using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Investigate and troubleshoot out-of-specification (OOS) results and deviations, implementing corrective and preventive actions (CAPAs).
• Maintain laboratory equipment, ensuring proper calibration and adherence to Good Manufacturing Practices (GMP).
• Review and approve analytical data and reports, ensuring compliance with regulatory requirements.
• Mentor and train junior analytical chemists and technicians on laboratory procedures and techniques.

Requirements

• M.Sc. or Ph.D. in Chemistry, Analytical Chemistry, or a related field.
• Minimum of 5 years of experience in pharmaceutical Quality Control (QC) or analytical development.
• Extensive experience with HPLC, GC, and wet chemistry techniques .
• Thorough understanding of GMP, ICH guidelines, and regulatory requirements in the pharmaceutical industry.
• Experience with method validation and stability studies.
• Strong analytical skills, attention to detail, and problem-solving capabilities.

Benefits

• Competitive salary and comprehensive benefits package including health and retirement plans.
• Opportunities for professional development and continuous learning in pharmaceutical sciences.
• Exposure to cutting-edge analytical technologies and methodologies.
• A structured and compliant work environment adhering to international standards.
• Collaborative team atmosphere focused on product quality and patient safety.
• Contribute to the delivery of safe and effective medicines.