Pharmaceutical QC Analyst - GMP/GLP Specialist

Placements24; Rustenburg; On-site; ZAR 450,000 - 600,000; Full time

Benefits offered by this job

Competitive salary

Health, disability & life insurance

Pension fund contribution

Paid time off and company holidays

Training & growth

Job summary

Placements24 is seeking a meticulous Quality Control Analyst for our Rustenburg facility to ensure pharmaceutical products meet quality, safety, and efficacy standards. You will conduct tests on raw materials, in-process samples, and finished products using HPLC, GC, and spectrophotometric methods.

The role requires a Bachelor's in Chemistry or Pharmaceutical Sciences, 2+ years in QC labs, strong documentation, and GMP/GLP knowledge; on-site position with a competitive salary and benefits.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, or related field.
• 2+ years in a pharmaceutical QC laboratory setting.
• Proficiency with analytical techniques and instrumentation (HPLC, GC, UV-Vis).
• GMP/GLP knowledge and strong documentation skills.

Responsibilities

• Conduct routine and non-routine analytical testing of raw materials, intermediates, and finished products.
• Operate and maintain laboratory instruments such as HPLC, GC, spectrophotometers, and dissolution apparatus.
• Analyze test results, document findings, and report deviations or out-of-spec results promptly.
• Participate in method development and validation activities for new procedures.
• Ensure GMP/GLP compliance in laboratory operations in Rustenburg.

Skills

Analytical testing

Laboratory instrumentation

HPLC

GC

UV-Vis

Documentation

Education

Bachelor's degree in Chemistry/Pharmaceutical Sciences

Tools

HPLC

GC

UV-Vis spectrophotometer

Dissolution apparatus

Job description

Placements24 is seeking a meticulous Quality Control Analyst for our Rustenburg facility to ensure pharmaceutical products meet quality, safety, and efficacy standards. You will conduct tests on raw materials, in-process samples, and finished products using HPLC, GC, and spectrophotometric methods.

The role requires a Bachelor's in Chemistry or Pharmaceutical Sciences, 2+ years in QC labs, strong documentation, and GMP/GLP knowledge; on-site position with a competitive salary and benefits.