Quality Control Analyst - Pharmaceuticals

Placements24; Mbombela (Nelspruit); On-site; ZAR 300,000 - 420,000; Full time

Benefits offered by this job

Competitive salary

Medical and pension benefits

On-the-job training

Safe laboratory environment

Collaborative team atmosphere

Job summary

Placements24 is seeking a meticulous Quality Control Analyst to join the laboratory team in Nelspruit (Mbombela). You will perform analytical testing on raw materials, in-process samples, and finished pharmaceutical products to ensure quality specifications and regulatory standards are met.

The role requires a Bachelor’s degree in Chemistry or Pharmacy and at least 2 years of QC experience, with proficiency in HPLC, GC, UV-Vis, and Karl Fischer titration, plus a strong GMP background and

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, or a related science discipline.
• Minimum of 2 years of experience as a Quality Control Analyst in the pharmaceutical industry.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration.

Responsibilities

• Conduct routine and non-routine analytical testing of raw materials, intermediates, and finished products using validated methods.
• Perform laboratory procedures such as chromatography (HPLC, GC), spectroscopy (UV-Vis, IR), and titration.
• Accurately record and document all testing results, ensuring compliance with laboratory procedures and GMP.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to schedules.
• Prepare analytical reports and certificates of analysis.
• Investigate out-of-specification (OOS) results and deviations, assisting in root cause analysis.

Skills

Analytical chemistry

GMP knowledge

Data accuracy

Attention to detail

Teamwork

Education

Bachelor's degree in Chemistry or Pharmacy

Tools

HPLC

GC

UV-Vis

Karl Fischer titration

Job description

About the Role

Our client is seeking a meticulous Quality Control Analyst to join their laboratory team in Nelspruit . You will perform a variety of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet established quality specifications and regulatory standards. This role requires a strong understanding of analytical chemistry techniques and a commitment to maintaining the integrity and safety of our pharmaceutical products. You will be an integral part of ensuring compliance with Good Manufacturing Practices (GMP) .

Key Responsibilities

• Conduct routine and non-routine analytical testing of raw materials, intermediates, and finished products using validated methods.
• Perform laboratory procedures such as chromatography (HPLC, GC), spectroscopy (UV-Vis, IR), and titration.
• Accurately record and document all testing results, ensuring compliance with laboratory procedures and GMP.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to schedules.
• Prepare analytical reports and certificates of analysis.
• Investigate out-of-specification (OOS) results and deviations, assisting in root cause analysis.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, or a related science discipline.
• Minimum of 2 years of experience as a Quality Control Analyst in the pharmaceutical industry.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, and Karl Fischer titration.
• Knowledge of GMP and laboratory best practices.
• Strong attention to detail and accuracy in data recording and analysis.
• Ability to work effectively both independently and as part of a team in the Nelspruit laboratory.

Benefits

• Competitive annual salary with potential for overtime pay.
• Comprehensive medical and pension benefits.
• Opportunities for on-the-job training and skill development in analytical methods.
• A structured and safe laboratory environment.
• Collaborative team atmosphere within a well-established pharmaceutical company .