Quality Control Analyst - Pharmaceuticals

Placements24; Mtubatuba Local Municipality; On-site; ZAR 300,000 - 420,000; Full time

Job summary

Placements24 seeks a detail-oriented Quality Control Analyst to join a pharmaceutical manufacturing facility in Richards Bay. You will perform routine analytical testing on raw materials, in-process samples, and finished products, ensuring GMP/GLP compliance and precise documentation.

The ideal candidate has a Bachelor's degree in Chemistry or Pharmacy and 1–3 years of QC experience, with proficiency in HPLC, GC, UV-Vis and wet chemistry, plus strong data integrity and teamwork skills,

Qualifications

• Bachelor's degree in Chemistry, Pharmacy or related science.
• 1–3 years in QC or analytical lab, preferably pharmaceutical.
• Proficiency with HPLC, GC, UV-Vis and wet chemistry.
• Strong GMP and GLP knowledge and data recording accuracy.

Responsibilities

• Perform routine analytical testing on raw materials, intermediates and finished goods.
• Operate and maintain laboratory equipment with proper calibration.
• Document testing results and observations in compliance with GMP/GLP.
• Investigate deviations and contribute to root-cause analyses and CoA preparation.

Skills

Analytical testing

HPLC

GC

UV-Vis

GLP

GMP

Data integrity

Attention to detail

Teamwork

Education

Bachelor's degree in Chemistry or Pharmacy

Tools

HPLC equipment

GC equipment

UV-Vis spectrophotometer

Job description

About the Role

Our client is seeking a detail-oriented Quality Control Analyst to join their manufacturing facility in Richards Bay . In this role, you will be responsible for ensuring that all pharmaceutical products meet the highest standards of quality and safety before they reach consumers. You will perform a variety of tests and analyses on raw materials, in-process samples, and finished goods, meticulously documenting your findings. This position is crucial for maintaining regulatory compliance and upholding our client's commitment to producing safe and effective medications.

Key Responsibilities

• Perform routine analytical testing on raw materials, intermediate products, and finished pharmaceutical goods using established methods.
• Operate and maintain laboratory equipment, ensuring calibration and functionality.
• Document all testing procedures, results, and observations accurately and thoroughly in compliance with GMP.
• Investigate deviations and out-of-specification (OOS) results, and participate in root cause analysis.
• Prepare Certificates of Analysis (CoA) for released products.
• Adhere strictly to safety protocols and good laboratory practices (GLP) within the Richards Bay facility.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, or a related scientific discipline.
• 1-3 years of experience in a Quality Control or analytical laboratory setting, preferably within the pharmaceutical industry.
• Proficiency with common analytical techniques such as HPLC, GC, UV-Vis spectrophotometry, and wet chemistry.
• Strong understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Excellent attention to detail and accuracy in data recording and analysis.
• Ability to work effectively independently and as part of a team in a manufacturing environment.

Benefits

• Competitive annual salary and potential for performance-based incentives.
• Comprehensive medical aid and retirement fund benefits.
• Opportunities for training and professional development in pharmaceutical quality control.
• A stable working environment within a reputable manufacturing plant in Richards Bay .
• Company-sponsored social events and team-building activities.