Senior Quality Control Analyst — Pharma Testing Expert

Placements24; Noord-Kaap; On-site; ZAR 600,000 - 900,000; Full time

Benefits offered by this job

Competitive salary

Health benefits

Training and development

Stable work environment

Impact on public safety

Job summary

Placements24 is seeking a highly skilled Senior Quality Control Analyst to join its laboratory team in Kimberley. The role focuses on performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with specifications and regulatory standards.

You will work with HPLC, GC, UV-Vis and wet chemistry, document results, calibrate equipment, investigate OOS findings, and assist with method validation and transfers in a GMP/GLP environment.

Qualifications

• Bachelor's degree in Chemistry or Analytical Chemistry.
• Minimum 5 years in QC lab, preferably pharma.
• Proficient with HPLC, GC, and dissolution testing.
• Strong GMP/GLP knowledge and documentation skills.
• Ability to work independently and in a team.

Responsibilities

• Perform analytical tests using HPLC, GC, UV-Vis, and wet chemistry.
• Analyze materials and finished products per SOPs.
• Document testing activities and observations.
• Calibrate and maintain lab equipment.
• Investigate OOS results and deviations, contributing to root cause analysis.
• Assist in method validation and transfer activities.

Skills

HPLC

GC

Dissolution testing

Attention to detail

Teamwork

Education

Bachelor's degree in Chemistry

Analytical Chemistry

Tools

HPLC System

GC System

Dissolution Apparatus

Job description

Placements24 is seeking a highly skilled Senior Quality Control Analyst to join its laboratory team in Kimberley. The role focuses on performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products to ensure compliance with specifications and regulatory standards.

You will work with HPLC, GC, UV-Vis and wet chemistry, document results, calibrate equipment, investigate OOS findings, and assist with method validation and transfers in a GMP/GLP environment.