Pharmaceutical Quality Control Analyst

Placements24; Soweto; On-site; ZAR 300,000 - 520,000; Full time

Benefits offered by this job

Medical aid

Retirement fund

On-the-job training

Supportive team

Soweto location

Job summary

Placements24 is seeking a diligent Pharmaceutical Quality Control Analyst to join the Soweto laboratory team. You will perform analytical tests on raw materials, intermediates and finished products to ensure quality and safety, using HPLC, GC, UV-Vis and titration.

The ideal candidate holds a Bachelor’s degree in Chemistry with 1–3 years of QC experience in a pharmaceutical setting, and demonstrates strong attention to detail and knowledge of GMP principles.

Qualifications

• Bachelor's degree in Chemistry or related science field.
• 1–3 years of pharmaceutical QC laboratory experience.
• Proficiency with HPLC/GC and spectrophotometers.
• Knowledge of USP/BP and GMP principles.
• Strong attention to detail and data integrity.

Responsibilities

• Perform analytical tests on raw materials, intermediates, and finished products using HPLC, GC, UV-Vis, and titration.
• Analyze results, document findings, and report deviations or OOS results.
• Prepare reagents, standards and samples for testing.
• Maintain equipment and calibrations in a GMP-compliant lab.
• Participate in method validation and transfers.
• Adhere to GMP and SOPs.

Skills

Analytical chemistry

Attention to detail

Data recording

GMP knowledge

Education

Bachelor's degree in Chemistry

Tools

HPLC

GC

UV-Vis spectrophotometer

Titration

Job description

About the Role

Our client is seeking a diligent and detail-oriented Pharmaceutical Quality Control Analyst to join their laboratory team in Soweto . This role is essential for performing a wide range of analytical tests on raw materials, intermediates, and finished pharmaceutical products to ensure they meet established quality and safety standards. You will work with advanced analytical instrumentation and adhere strictly to GMP and SOP guidelines. The ideal candidate has a strong foundation in analytical chemistry and a commitment to maintaining product integrity within a regulated pharmaceutical environment, contributing to the overall quality assurance of life-saving medications.

Key Responsibilities

• Perform various analytical tests on raw materials, packaging components, and finished products using techniques such as HPLC, GC, UV-Vis, and titration.
• Analyze test results, accurately document findings, and report any deviations or out-of-specification (OOS) results.
• Prepare reagents, standards, and samples for testing.
• Maintain laboratory equipment, perform calibrations, and ensure compliance with laboratory safety procedures.
• Participate in method validation and transfer activities as required.
• Adhere to all Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs).

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related science field.
• 1-3 years of experience in a pharmaceutical Quality Control laboratory.
• Proficiency with common analytical instruments (e.g., HPLC, GC, spectrophotometers).
• Knowledge of pharmacopoeial standards (e.g., USP, BP) and GMP principles.
• Strong attention to detail and accuracy in data recording and reporting.

Benefits

• Competitive salary and potential for annual bonuses.
• Medical aid and retirement fund benefits.
• On-the-job training and opportunities for skill development.
• A supportive and collaborative work environment in Soweto .
• Contribution to the production of essential pharmaceutical products.