Quality Control Analyst

Placements24; Benoni; On-site; ZAR 420,000 - 540,000; Full time

Benefits offered by this job

Medical aid

Retirement fund

Training opportunities

Performance bonus

Job security

Modern labs

Team environment

Paid time off

Job summary

Placements24 is seeking a meticulous Quality Control Analyst for a pharmaceutical manufacturer in Benoni, Gauteng. The role focuses on analytical testing of materials and finished products in a GMP environment, with strict documentation and data integrity required.

The candidate should have a bachelor’s degree in Chemistry or related field and at least 3 years of QC lab experience, with hands-on HPLC and GC experience and strong attention to detail.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field.
• 3+ years' experience in pharmaceutical QC lab.
• Hands-on with HPLC and GC mandatory.
• Familiarity with GMP and QA/QC processes.
• Accurate data recording and analysis.

Responsibilities

• Perform routine and non-routine analytical tests on raw materials, in-process samples, and finished products using HPLC, GC, UV-Vis, dissolution apparatus, and Karl Fischer titrator.
• Prepare reagents, solutions, and standards for testing.
• Record and document test results, observations, and deviations in notebooks and electronic systems.
• Calibrate, maintain, troubleshoot lab equipment to ensure accuracy.
• Ensure GMP, SOPs and safety guidelines are followed.

Skills

HPLC

GC

UV-Vis spectrophotometer

Dissolution testing

Karl Fischer titration

GMP

Data recording

Education

Bachelor's degree in Chemistry

Tools

HPLC instrumentation

GC instrumentation

Job description

About the Role

Our client, a reputable pharmaceutical manufacturer, is seeking a meticulous and technically skilled Quality Control Analyst to join their operations in Benoni, Gauteng. This role is fundamental to ensuring the consistent quality and safety of our client's pharmaceutical products. The analyst will be responsible for performing a wide range of analytical tests on raw materials, intermediates, and finished products, meticulously documenting results, and ensuring compliance with stringent quality standards and regulatory requirements. This is a hands‑on laboratory position requiring a keen eye for detail and a strong understanding of analytical techniques within a Good Manufacturing Practice (GMP) environment. We are dedicated to producing high-quality medicines and require a dedicated professional to uphold our commitment.

Key Responsibilities

• Conduct routine and non‑routine analytical testing of raw materials, in‑process samples, and finished pharmaceutical products using various laboratory instruments (e.g., HPLC, GC, UV‑Vis spectrophotometer, dissolution apparatus, Karl Fischer titrator).
• Prepare reagents, solutions, and standards required for analytical testing.
• Accurately record and document all test results, observations, and deviations in laboratory notebooks and electronic systems.
• Verify and review data generated by other analysts, ensuring accuracy and compliance with specifications.
• Calibrate, maintain, and troubleshoot laboratory equipment to ensure proper functioning and accuracy.
• Ensure all activities are performed in accordance with GMP, SOPs, and safety guidelines.
• Participate in method validation and transfer activities as required.
• Report any out‑of‑specification (OOS) results or deviations promptly to supervisors.
• Contribute to internal audits and continuous improvement initiatives within the QC department.
• Maintain a clean and organized laboratory environment.

Requirements

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 3 years of experience in a pharmaceutical Quality Control laboratory environment.
• Hands‑on experience with essential analytical techniques such as HPLC and GC is mandatory.
• Familiarity with GMP regulations and quality control procedures in the pharmaceutical industry.
• Proficiency in laboratory techniques and good laboratory practices.
• Strong attention to detail and accuracy in data recording and analysis.
• Good understanding of basic chemistry principles.
• Ability to interpret analytical data and identify deviations.
• Effective written and verbal communication skills.
• Ability to work both independently and as part of a team in a fast‑paced environment.
• Must be legally authorized to work in South Africa.

Benefits

• Competitive annual salary.
• Comprehensive medical aid and retirement fund.
• Opportunities for training and professional development.
• Performance‑related bonuses.
• Secure employment within a stable industry.
• Access to modern laboratory facilities.
• Supportive team environment.
• Paid time off.