Pharma QC Analyst - Precision Lab Testing & Compliance

Placements24

Klerksdorp

On-site

ZAR 350,000 - 520,000

Full time

3 days ago
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Benefits offered by this job

Medical aid and retirement fund
Generous annual leave
On-site parking

Job summary

Placements24 in Klerksdorp is seeking a meticulous Quality Control Analyst to join our pharmaceutical client’s team. The role focuses on analytical testing of raw materials and finished products, ensuring quality and regulatory compliance in a GMP/GDP environment.

You will perform HPLC, GC, UV-Vis and other analyses, document results accurately, support method validation, and assist during internal audits and regulator inspections.

Qualifications

  • Bachelor of Science in Chemistry, Biochemistry, Pharmacy or related life science discipline.
  • Minimum of 3 years as a QC Analyst in pharmaceutical industry, focused on raw material testing.
  • Strong experience with analytical techniques (HPLC, GC, UV-Vis, IR spectroscopy) and wet chemistry methods.
  • Knowledge of GMP, GLP and pharmacopeial standards (USP/EP/BP).

Responsibilities

  • Perform analytical tests on incoming raw materials, intermediates, and finished products.
  • Document testing procedures and results in accordance with GLP and GMP.
  • Investigate out-of-specification (OOS) results and participate in root-cause investigations.
  • Review and approve analytical data for raw materials and components.
  • Maintain a clean, safe laboratory and assist in internal audits and regulator inspections.

Skills

HPLC
GC
UV-Vis
IR spectroscopy
Wet chemistry

Education

Bachelor of Science in Chemistry/Biochemistry/Pharmacy

Tools

LIMS

Job description

Placements24 in Klerksdorp is seeking a meticulous Quality Control Analyst to join our pharmaceutical client’s team. The role focuses on analytical testing of raw materials and finished products, ensuring quality and regulatory compliance in a GMP/GDP environment.

You will perform HPLC, GC, UV-Vis and other analyses, document results accurately, support method validation, and assist during internal audits and regulator inspections.

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