Quality Control Analyst – On-Site Lab (Welkom)

Placements24; Willows (CA); Sur place; USD 21 000 - 31 000; Plein temps

Avantages offerts par ce poste

Medical aid

Provident fund

On-site facility

Résumé du poste

Placements24 seeks a diligent Pharmaceutical Quality Control Analyst for our Welkom, Free State facility. You will perform routine analytical testing on raw materials, intermediates, and finished products using HPLC, GC, UV-Vis, and dissolution methods.

You will record data, support investigations of OOS results, and ensure GMP/GLP compliance. The role emphasizes meticulous documentation, teamwork, and opportunities for method validation and continuous improvement.

Qualifications

• Bachelor's degree in Chemistry, Pharmacy, or related scientific discipline.
• 2–3 years of experience in a pharmaceutical Quality Control laboratory.
• Hands-on experience with HPLC and GC.
• Familiarity with FTIR, dissolution testing, and Karl Fischer titration is advantageous.
• Knowledge of GMP and regulatory requirements for pharmaceutical manufacturing.
• Strong understanding of analytical principles and laboratory techniques.
• Excellent documentation skills and attention to detail.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.
• Good problem-solving skills and the ability to troubleshoot analytical methods and instrumentation.
• Proficiency in data entry and MS Office.

Responsabilités

• Perform routine analytical testing of raw materials, intermediates, and finished products according to established methods.
• Operate and maintain analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Prepare reagents, standards, and samples for analysis.
• Record test results accurately in laboratory notebooks and LIMS.
• Investigate out-of-specification results and deviations, participating in root cause analysis.
• Review and verify analytical data generated by other QC analysts.
• Ensure GMP/GLP compliance and adherence to internal quality policies.
• Participate in method validation and transfer activities as required.
• Maintain laboratory equipment and calibration schedules.
• Contribute to continuous improvement initiatives within the Quality Control department.

Connaissances

HPLC

GC

Analytical testing

Documentation

Problem solving

MS Office

Teamwork

Formation

Bachelor's degree in Chemistry/Pharmacy or related field

Outils

FTIR

Dissolution testing

Karl Fischer titration

Description du poste

Placements24 seeks a diligent Pharmaceutical Quality Control Analyst for our Welkom, Free State facility. You will perform routine analytical testing on raw materials, intermediates, and finished products using HPLC, GC, UV-Vis, and dissolution methods.

You will record data, support investigations of OOS results, and ensure GMP/GLP compliance. The role emphasizes meticulous documentation, teamwork, and opportunities for method validation and continuous improvement.