QC Analayst

SUMMARY:
Our client in the pharmaceutical industry is looking for QC lab analyst to start asap for a 3 months fixed contract  based KZN.  If you meet the below requirements please send us your CV.

The QC Lab Analyst is responsible for performing analytical testing of raw materials, in-process samples, finished products, stability samples, and water systems in accordance with approved specifications, GMP requirements, and standard operating procedures (SOPs). The role supports product quality, regulatory compliance, and continuous improvement within the laboratory environment.

Requirements:

• Test raw materials, packaging materials, finished products, and stability samples according to approved methods.
• Prepare reagents, standards, volumetric solutions, and mobile phases.
• Operate, calibrate, troubleshoot, and maintain laboratory instruments.
• Review analytical data for accuracy and completeness before submission.
• Record and maintain laboratory documentation in compliance with GMP and data integrity requirements.
• Investigate out-of-specification (OOS), out-of-trend (OOT), and laboratory deviations.
• Participate in method validation, method verification, and method transfer activities.
• Ensure compliance with:
  • GMP
  • GLP
  • SOPs
  • Pharmacopoeial requirements (USP, BP, EP)
• Support internal and external audits and regulatory inspections.
• Maintain laboratory cleanliness and safety standards.
• Assist with stability studies and environmental monitoring where required

• Bachelor’s Degree or National Diploma in:
  • Chemistry
  • Analytical Chemistry
  • Biochemistry
  • Pharmaceutical Sciences
  • Microbiology (if applicable)

Experience

• 2–3 years’ experience in a pharmaceutical QC laboratory.
• Experience working in a GMP-regulated environment.
• Hands-on experience with HPLC is typically essential.

POSITION INFO: