Pharmaceutical Quality Control Analyst

Placements24

Klerksdorp

On-site

ZAR 350,000 - 550,000

Full time

5 days ago
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Benefits offered by this job

Competitive salary
Health, dental, and vision insurance
Pension plan contributions
On-the-job training
Stable work environment in Klerksdorp

Job summary

Placements24 is seeking a Pharmaceutical Quality Control Analyst for a manufacturing facility in Klerksdorp. The role focuses on rigorous testing of materials and products using HPLC, GC, UV-Vis, and titrations, with emphasis on GMP-compliant documentation and COA preparation.

The candidate should hold a Bachelors in Chemistry/Analytical Chemistry/Pharmacy and have 2–4 years of QC experience, strong attention to detail, and good teamwork skills.

Qualifications

  • Bachelor's degree in Chemistry/Analytical Chemistry/Pharmacy.
  • 2–4 years of QC laboratory experience in pharmaceutical manufacturing.
  • Strong GMP knowledge and good documentation practices.

Responsibilities

  • Perform analytical testing on raw materials, intermediates and finished products using HPLC, GC, UV-Vis and titrations.
  • Analyze and interpret results against established specifications and quality standards.
  • Document testing procedures, results and observations per SOPs and GMP.
  • Prepare Certificates of Analysis for released batches.
  • Maintain and calibrate laboratory equipment; ensure GxP compliance.
  • Investigate OOS results and support deviation investigations as needed.

Skills

Attention to detail
Documentation skills
Teamwork

Education

Bachelor's degree in Chemistry/Analytical Chemistry/Pharmacy

Tools

HPLC
GC
Dissolution testers
GMP knowledge

Job description

About the Role

Our client is seeking a dedicated Pharmaceutical Quality Control Analyst to join their manufacturing facility in Klerksdorp . This role is essential for ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products according to established specifications and standard operating procedures (SOPs). The ideal candidate is highly meticulous, possesses strong analytical skills, and is committed to upholding the highest quality standards in pharmaceutical manufacturing. This position offers a great opportunity to contribute to a critical function within a reputable pharmaceutical company, ensuring compliance with regulatory requirements and product integrity.

Key Responsibilities
  • Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titrations).
  • Analyze and interpret test results, comparing them against established specifications and quality standards.
  • Document all testing procedures, results, and observations accurately and in compliance with GMP requirements.
  • Prepare Certificates of Analysis (CoAs) for released batches of products.
  • Maintain laboratory equipment, calibrate instruments, and ensure compliance with GxP guidelines.
  • Investigate Out-of-Specification (OOS) results and participate in deviation investigations as needed.
Requirements
  • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific field.
  • 2-4 years of experience in a pharmaceutical Quality Control (QC) laboratory setting.
  • Proficiency with analytical instrumentation such as HPLC , GC, and dissolution testers.
  • Solid understanding of Good Manufacturing Practices (GMP) and pharmaceutical quality systems.
  • Strong attention to detail, accuracy, and ability to follow detailed procedures.
  • Good documentation skills and ability to work effectively in a team-oriented environment.
Benefits
  • Competitive annual salary with potential for annual bonuses.
  • Comprehensive health, dental, and vision insurance coverage.
  • Pension fund contributions.
  • On-the-job training and opportunities for career advancement within the quality department.
  • Stable work environment in Klerksdorp , contributing to vital healthcare products.
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