Pharmaceutical Quality Control Analyst

Placements24; Willows (CA); On-site; USD 21,000 - 31,000; Full time

Benefits offered by this job

Medical aid

Provident fund

On-site facility

Job summary

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.

Responsibilities

• 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.

Skills

HPLC

GC

Analytical testing

Documentation

Problem solving

MS Office

Teamwork

Education

Bachelor's degree in Chemistry/Pharmacy or related field

Tools

FTIR

Dissolution testing

Karl Fischer titration

Job description

About the Role

Our client, a respected pharmaceutical manufacturer, is seeking a diligent and analytical Pharmaceutical Quality Control Analyst to join their team in Welkom, Free State . This role is critical in ensuring that all manufactured products meet stringent quality standards and regulatory requirements. The analyst will perform a variety of laboratory tests on raw materials, in-process samples, and finished products using sophisticated analytical instrumentation. The successful candidate will be meticulous, possess strong laboratory skills, and be committed to maintaining the highest levels of product quality and safety. This position offers a great opportunity to contribute to the production of essential medicines within a supportive and regulated environment.

Key Responsibilities

• Perform routine analytical testing of raw materials, intermediates, and finished pharmaceutical products according to established methods and specifications.
• 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 and meticulously in laboratory notebooks and LIMS (Laboratory Information Management System).
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Review and verify analytical data generated by other QC analysts.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and internal quality policies.
• Participate in method validation and transfer activities as required.
• Maintain laboratory equipment and ensure calibration schedules are adhered to.
• Contribute to continuous improvement initiatives within the Quality Control department.

Requirements

• Bachelor's degree in Chemistry, Pharmacy, or a related scientific discipline.
• Minimum of 2-3 years of experience in a pharmaceutical Quality Control laboratory.
• Hands-on experience with HPLC and GC is essential.
• Familiarity with other analytical techniques like 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 basic computer skills (e.g., MS Office).

Benefits

Our client offers a competitive salary, medical aid, and provident fund benefits. Employees have access to ongoing training and development opportunities, fostering career growth within the pharmaceutical quality sector. The role is based in our well-equipped laboratory facility in Welkom, Free State . We promote a safety-conscious culture and provide a stable working environment. This position requires on-site presence to ensure laboratory operations and quality control standards are maintained effectively.