Pharma QC Analyst — Modern Lab, Growth & Benefits

Placements24

Bellville

Hybride

ZAR 420 000 - 660 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Competitive salary
Medical aid
Retirement fund
Training opportunities
Modern laboratory facilities
Parking

Résumé du poste

Placements24 is seeking a detail-oriented Quality Control Analyst to join a pharmaceutical client in Centurion, Gauteng. The role covers qualitative and quantitative testing of raw materials, in‑process samples, and finished products to ensure GMP/GLP compliance and pharmacopeial standards.

You will use HPLC, GC, UV-Vis, FTIR, and dissolution methods, maintain data in LIMS, and assist with method validation and investigations.

Qualifications

  • Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences or related field.
  • Minimum of 3 years of experience in a pharmaceutical QC lab.
  • Hands-on with HPLC and GC; knowledge of GMP/GLP and regulatory guidelines.

Responsabilités

  • Perform qualitative and quantitative analytical tests on raw materials, intermediates, and finished products using HPLC, GC, UV-Vis, FTIR and dissolution testing.
  • Prepare reagents, standards, and samples for analysis following established procedures.
  • Document results accurately in laboratory notebooks and electronic systems (LIMS).
  • Calibrate, maintain, and troubleshoot laboratory instruments to ensure performance and compliance.
  • Review and interpret data, report deviations to supervisors, and participate in method validation/transfer activities.

Connaissances

Analytical thinking
Problem solving
Detail oriented
Communication
Teamwork

Formation

Bachelor's degree in Chemistry or related field

Outils

HPLC
GC
LIMS
UV-Vis
FTIR

Description du poste

Placements24 is seeking a detail-oriented Quality Control Analyst to join a pharmaceutical client in Centurion, Gauteng. The role covers qualitative and quantitative testing of raw materials, in‑process samples, and finished products to ensure GMP/GLP compliance and pharmacopeial standards.

You will use HPLC, GC, UV-Vis, FTIR, and dissolution methods, maintain data in LIMS, and assist with method validation and investigations.

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