Pharma QC Analyst: Hands-on Lab & GMP Quality

Placements24

Noord-Kaap

On-site

ZAR 350,000 - 500,000

Full time

12 days ago
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Benefits offered by this job

Competitive salary
Benefits package
Professional development
Hands-on instrumentation experience
Safe and well-equipped lab

Job summary

Placements24 is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join our laboratory team in Kimberley. You will perform a variety of chemical and physical tests on raw materials, in-process samples, and finished products in accordance with established specifications and SOPs.

The ideal candidate has a foundation in analytical chemistry, hands-on experience with GMP-compliant QA/QC environments, and a commitment to product safety and efficacy through rigorous

Qualifications

  • Bachelor's degree in Chemistry, Pharmaceutical Sciences or related field.
  • Minimum 2 years of QC laboratory experience in pharma.
  • Experience with analytical techniques like HPLC, GC, titration and spectrophotometry.

Responsibilities

  • Perform analytical testing on raw materials, intermediates, and finished products using laboratory techniques.
  • Prepare reagents, solutions, and standards for testing.
  • Document results and calculations in lab notebooks and electronic systems.
  • Calibrate, maintain, and troubleshoot laboratory equipment.
  • Review data, identify out-of-spec results, and participate in investigations.
  • Adhere to GMP, safety protocols, and SOPs.

Skills

Analytical chemistry
GMP knowledge
Attention to detail
Documentation
Independent work
Team collaboration

Education

Bachelor's degree in Chemistry or Pharmaceutical Sciences

Tools

HPLC
GC
Titration
Spectrophotometry

Job description

Placements24 is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join our laboratory team in Kimberley. You will perform a variety of chemical and physical tests on raw materials, in-process samples, and finished products in accordance with established specifications and SOPs.

The ideal candidate has a foundation in analytical chemistry, hands-on experience with GMP-compliant QA/QC environments, and a commitment to product safety and efficacy through rigorous

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