Pharma Quality Control Analyst: Elevate Lab Compliance

Placements24

Upington

On-site

ZAR 240,000 - 420,000

Full time

3 days ago
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Benefits offered by this job

Medical aid
Pension fund
Professional development
Competitive salary

Job summary

Placements24 in Upington, Northern Cape, is seeking a Quality Control Analyst to join the pharmaceutical lab team. You will perform chemical tests on raw materials, in-process samples, and finished products to ensure adherence to specifications and regulatory standards.

The role requires a degree in chemistry-related field and 1–2 years in a regulated lab, with hands-on experience in HPLC, GC, UV-Vis and GLP/GMP practices, and the ability to work both independently and within a team.

Qualifications

  • Bachelor's degree in Chemistry, Biochemistry, Pharmacy or a related field.
  • 1–2 years in a Quality Control laboratory, preferably pharma.
  • Experience with analytical methods (HPLC, GC, wet chemistry).
  • Knowledge of GMP and regulatory requirements.

Responsibilities

  • Perform routine analytical testing on raw materials, in-process samples, and finished products.
  • Prepare reagents, standards and calibrations for tests.
  • Operate and maintain QC instruments and ensure calibration records.
  • Document results in notebooks and LIMS with accuracy.
  • Analyze data, report deviations and support investigations.
  • Contribute to method validation and GLP/GMP compliance.

Skills

HPLC
GC
UV-Vis
FTIR
LIMS
MS Office
Analytical chemistry

Education

Bachelor's degree in Chemistry/Biochemistry/Pharmacy

Tools

HPLC
GC
UV-Vis
FTIR
LIMS
MS Office

Job description

Placements24 in Upington, Northern Cape, is seeking a Quality Control Analyst to join the pharmaceutical lab team. You will perform chemical tests on raw materials, in-process samples, and finished products to ensure adherence to specifications and regulatory standards.

The role requires a degree in chemistry-related field and 1–2 years in a regulated lab, with hands-on experience in HPLC, GC, UV-Vis and GLP/GMP practices, and the ability to work both independently and within a team.

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