Quality Control (QC) Analyst

Avacare Health Group; Cape Town; On-site; ZAR 200,000 - 300,000; Full time

Job summary

A pharmaceutical company in Cape Town is seeking an experienced Quality Control (QC) Analyst to ensure the highest quality standards for raw materials and products. You will conduct various tests, maintain laboratory equipment, and support quality assurance processes. Ideal candidates should have a tertiary qualification in a relevant field and 3-4 years of experience in QC, alongside strong analytical skills. Applications can be sent to [e-mail].

Qualifications

• 3-4 years’ experience as a QC Analyst in pharmaceuticals or manufacturing.
• Hands-on experience with analytical and microbiological testing.
• Strong knowledge of GMP and regulatory compliance.

Responsibilities

• Conduct tests on raw materials and finished products.
• Prepare and interpret test results accurately.
• Support continuous improvement in QC processes.

Skills

Analytical Chemistry

Microbiology

Attention to Detail

Problem-solving

Communication Skills

Education

Tertiary qualification in Chemistry, Biotechnology, or Microbiology

Tools

HPLC

Laboratory Equipment

Job description

Overview

Job Title: Quality Control (QC) Analyst

Location: Cape Town, Ndabeni

Contract Type: Permanent

About the Role

Barrs Pharmaceutical Industries (Pty) Ltd is seeking a skilled and experienced Quality Control Analyst to join our Quality team. This role is key in ensuring the highest quality standards for our raw materials, in-process samples, and finished products.

Responsibilities

• Conduct raw material, in-process, stability, and finished product testing.
• Perform analytical and microbiological testing in compliance with SOPs and GMP standards.
• Operate and maintain laboratory equipment including HPLC, density meter, pH meter, potentiometer, Karl Fischer, conductivity meter, and other analytical instruments.
• Prepare, record, and interpret test results accurately and on time.
• Support continuous improvement in QC processes and maintain laboratory documentation.
• Assist in investigations, deviations, and reporting as required.

Qualifications & Experience

• Tertiary qualification in Chemistry, Biotechnology, Microbiology or a related field.
• 3–4 years’ experience as a QC Analyst in the pharmaceutical or manufacturing industry.
• Hands-on experience with raw material testing, analytical chemistry, microbiology, and stability testing.
• Proficiency in operating HPLC and other key analytical equipment.
• Strong knowledge of GMP, GLP, and regulatory compliance.

Key Competencies

• High attention to detail and accuracy.
• Strong problem-solving and analytical skills.
• Ability to work independently and as part of a team.
• Excellent communication and reporting skills.

How to Apply

Interested candidates are invited to submit their CV and supporting documents to [e-mail]

Closing date

Closing date: 19 September 2025

Please note

Only shortlisted candidates will be contacted. Should you not hear from us within 2 weeks after the closing date of applications, please consider your application unsuccessful.