Quality Control Analyst

Placements24; Noord-Kaap; On-site; ZAR 360,000 - 480,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Retirement fund

Hands-on training

Stable laboratory environment

Culture of precision

Job summary

Placements24 is seeking a diligent Quality Control Analyst to join their laboratory team in Kimberley, South Africa. You will perform analytical testing on raw materials, in-process samples, and finished pharmaceuticals to ensure quality and patient safety, using HPLC, GC, UV-Vis, and dissolution testing, while adhering to GLP and GMP.

The role requires a bachelor's degree in Chemistry, Biochemistry, Pharmacy or related field and at least two years of QC experience in pharma.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy or related scientific discipline.
• Minimum 2 years of experience as a Quality Control Analyst in the pharmaceutical industry.
• Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, and dissolution testers.
• Knowledge of GLP and GMP.

Responsibilities

• Perform analytical testing of raw materials, intermediates, and finished products using various laboratory techniques (HPLC, GC, spectroscopy).
• Analyze test results, compare against specifications, and document findings in notebooks and electronic systems.
• Investigate Out-of-Specification (OOS) results and determine root causes with relevant teams.
• Calibrate and maintain laboratory equipment for accuracy.
• Prepare standard solutions and reagents required for testing.
• Participate in method validation and transfer activities as needed.

Skills

Analytical skills

Problem solving

Attention to detail

Teamwork

Education

Bachelor's degree in Chemistry/Biochemistry/Pharmacy or related

Tools

HPLC

GC

UV-Vis

Dissolution testers

Job description

About the Role

Our client is seeking a diligent and analytical Quality Control Analyst to join their laboratory team in Kimberley. This position is responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet established quality standards and specifications. You will play a vital role in maintaining product integrity and ensuring patient safety through accurate and timely testing. This role requires a strong scientific foundation and a commitment to upholding rigorous quality control procedures.

Key Responsibilities

• Perform analytical testing of raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, spectroscopy).
• Analyze test results, compare them against specifications, and document findings accurately in laboratory notebooks and electronic systems.
• Identify and investigate Out-of-Specification (OOS) results, collaborating with relevant teams to determine root causes.
• Calibrate and maintain laboratory equipment to ensure optimal performance and accuracy.
• Prepare standard solutions and reagents required for testing.
• Participate in method validation and transfer activities as needed.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific discipline.
• Minimum of 2 years of experience as a Quality Control Analyst in the pharmaceutical industry.
• Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, and dissolution testers.
• Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Strong analytical and problem-solving skills, with excellent attention to detail.
• Ability to work effectively both independently and as part of a team.

Benefits

• Competitive annual salary and potential for overtime pay.
• Comprehensive medical aid and retirement fund benefits.
• Opportunities for hands-on training and skill development in pharmaceutical analysis.
• A stable and safe laboratory environment.
• A culture focused on precision, quality, and scientific integrity.