QC Analyst Graduate Positions (x2)

Avacare Health Group; Cape Town; On-site; ZAR 150,000 - 220,000; Full time

Job summary

A leading pharmaceutical manufacturer in Cape Town is offering an exciting opportunity for recent graduates to join their Quality Control team as QC Analysts. You will perform analytical tests on raw materials and finished products to ensure compliance with quality standards. Ideal candidates are detail-oriented and eager to learn in a dynamic environment. This role is office-based with a closing date for applications on 30 June 2025.

Qualifications

• Recently qualified graduates with no required prior work experience.
• Strong attention to detail and good record-keeping skills.
• Willingness to learn in a regulated, fast-paced environment.

Responsibilities

• Conduct routine analysis using various analytical techniques.
• Perform method development and validation activities.
• Collaborate with departments to support product development.

Skills

Attention to detail

Good communication skills

Teamwork skills

Education

Qualification in Analytical Chemistry

Pharmaceutical Sciences

Biotechnology

Job description

Job Opportunity : QC Analyst Graduate Positions (x2)

Barrs Pharmaceuticals Industries (Pty) Ltd - A part of Avacare Health Group

Location : Ndabeni, Cape Town, South Africa

Position Type : Fixed Term

Barrs Pharmaceuticals is offering an exciting opportunity for two recently qualified graduates to join our team as Quality Control (QC) Analysts.

As a leading pharmaceutical manufacturer, we are committed to developing talent and driving innovation through high-quality standards. This graduate opportunity is ideal for individuals eager to gain hands-on experience and grow their careers in pharmaceutical quality control.

Overview

Purpose of the job : We are seeking a highly motivated and detail-oriented QC Analyst to join our Quality Control team. The successful candidate will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products to ensure they meet established quality standards and regulatory requirements.

Key Responsibilities :

• Conduct routine and non-routine analysis of raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Perform method development, validation, and transfer activities.
• Maintain and calibrate laboratory instruments and equipment.
• Prepare and review analytical reports, standard operating procedures (SOPs), and other quality documents.
• Ensure compliance with GMP, GLP, and other regulatory requirements.
• Investigate and resolve analytical issues and non-conformances.
• Participate in internal and external audits and inspections.
• Collaborate with other departments to support product development and manufacturing activities.

Requirements :

• A completed qualification in Analytical Chemistry, Pharmaceutical Sciences, Biotechnology, or a related field.
• No prior work experience required, but any lab-based training or internship will be advantageous.
• Strong attention to detail and good record-keeping skills.
• Willingness to learn and work in a regulated, fast-paced environment.
• Good communication and teamwork skills.

Closing date for applications: 30 June 2025

Location : Office-based

How to Apply :

Please send your CV and cover letter to [email address] with the subject line "QC Analyst Application".

Required Experience :

Key Skills: Computer skills, IT Audit, CAD/CAM, ABAP, Exterior Designing, HR Operations

Employment Type : Contract

Experience : N/A

Vacancy : 1