Quality Control Analyst

Placements24; Randfontein; On-site; ZAR 300,000 - 420,000; Full time

Benefits offered by this job

Health benefits

Training opportunities

Retirement plan

Job summary

Placements24 is seeking a Quality Control Analyst to join a pharmaceutical manufacturing team in Rustenburg. The role ensures quality and safety of products by conducting tests on materials, in-process samples, and finished goods, with meticulous documentation.

Ideal candidates have a chemistry/biochemistry/pharmacy background and at least 2 years in QC/analytical labs, with hands-on experience in HPLC, GC, UV-Vis, and titration, plus GMP/GLP knowledge.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or related field.
• Minimum of 2 years of experience in a Quality Control or analytical laboratory in the pharmaceutical industry.
• Proficiency with analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Understanding of GMP and GLP principles.

Responsibilities

• Perform routine laboratory tests on raw materials, intermediates, and finished pharmaceutical products using established methods and instrumentation.
• Analyze test results, compare them to established specifications, and report any deviations or out-of-specification results.
• Maintain laboratory equipment, ensure proper calibration, and adhere to GLP and safety requirements.
• Accurately document all testing procedures, results, and observations in laboratory notebooks and electronic systems.
• Participate in method validation and verification activities as required.

Skills

Laboratory testing

Analytical thinking

Documentation

Team player

Education

Bachelor's degree (Chemistry/Biochemistry/Pharmacy)

Tools

HPLC

GC

UV-Vis spectroscopy

Titration

Job description

About the Role

Our client seeks a diligent Quality Control Analyst to join their pharmaceutical manufacturing team in Rustenburg . This role is integral to ensuring the consistent quality and safety of all manufactured pharmaceutical products. You will perform a variety of laboratory tests and analyses on raw materials, in-process samples, and finished goods, meticulously documenting all findings. Your keen attention to detail and commitment to upholding the highest quality standards will directly impact the efficacy and safety of medications reaching patients, contributing to the company's reputation for excellence in pharmaceutical manufacturing within the North West province.

Key Responsibilities

• Perform routine laboratory tests on raw materials, intermediates, and finished pharmaceutical products using established methods and instrumentation.
• Analyze test results, compare them to established specifications, and report any deviations or out-of-specification results.
• Maintain laboratory equipment, ensure proper calibration, and adhere to all safety and Good Laboratory Practices (GLP).
• Accurately document all testing procedures, results, and observations in laboratory notebooks and electronic systems.
• Participate in method validation and verification activities as required.

Requirements

• Bachelor's degree in Chemistry, Biochemistry, Pharmacy, or a related scientific field.
• Minimum of 2 years of experience in a Quality Control or analytical laboratory setting within the pharmaceutical industry.
• Proficiency with analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Strong attention to detail and ability to work independently and as part of a team.

Benefits

• Competitive salary and benefits package.
• Opportunities for training and professional development in pharmaceutical quality assurance.
• Stable and secure employment in a growing industry.
• Positive and collaborative work environment focused on product integrity.
• Health and retirement benefits.