Quality Control Analyst - Pharmaceutical

Placements24; Gauteng; On-site; ZAR 420,000 - 540,000; Full time

Benefits offered by this job

Competitive salary

Medical benefits

Retirement benefits

Training and growth

Annual leave

Employee assistance

Job summary

Placements24 in Gauteng seeks a meticulous Quality Control Analyst to join the QA/QC team in Tembisa. You will perform analytical testing on raw materials, intermediates, and finished pharmaceutical products, ensuring compliance with GLP and GMP standards.

The role requires a Chemistry-related bachelor's degree and at least 3 years in a pharmaceutical QC lab, with hands-on experience in HPLC/GC and strict SOP adherence. On-site position with opportunities for professional growth.

Qualifications

• Bachelor's degree in Chemistry or related field.
• Minimum 3 years in pharmaceutical QC lab.
• Proficient with HPLC and GC instruments.
• Strong GMP/GLP knowledge and SOP discipline.
• Detail-oriented with meticulous record-keeping.
• On-site work in Tembisa, SA.

Responsibilities

• Perform routine and non-routine analytical testing of materials and products.
• Operate and maintain HPLC, GC, UV-Vis, and dissolution instruments.
• Document testing results and deviations per GLP and GMP.
• Investigate OOS results and assist with CAPA.
• Prepare Certificates of Analysis (CoA) and QC docs.
• Support method validation and transfer activities.

Skills

Analytical testing

HPLC/GC

GLP/GMP

SOP compliance

Documentation

Detail-oriented

Education

Bachelor's degree in Chemistry/Analytical Chemistry/Pharmacy

Tools

HPLC

GC

UV-Vis

Dissolution testing

Job description

About the Role

Our client seeks a meticulous and detail-oriented Quality Control Analyst to join their vital operations in Tembisa . This position plays a critical role in ensuring that all pharmaceutical products manufactured meet the highest standards of safety, efficacy, and quality. You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products. The successful candidate will be committed to maintaining stringent quality control procedures and contributing to the overall integrity of the company's product portfolio, working within a dedicated quality assurance department.

Key Responsibilities

• Perform routine and non-routine analytical testing of raw materials, intermediates, and finished pharmaceutical products using established methods.
• Operate and maintain laboratory equipment, including HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
• Accurately document all testing results, deviations, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Investigate out-of-specification (OOS) results and participate in root cause analysis to identify and implement corrective and preventive actions.
• Prepare Certificates of Analysis (CoA) and other quality control documentation as required.
• Participate in method validation and transfer activities for new or existing analytical methods.

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline.
• Minimum of 3 years of experience in a pharmaceutical Quality Control laboratory setting.
• Proficiency in operating and maintaining common analytical instruments such as HPLC and GC.
• Strong understanding of GMP , GLP, and relevant regulatory guidelines.
• Excellent attention to detail and ability to meticulously follow standard operating procedures (SOPs).
• Resides in or near Tembisa , with the ability to work on-site in a laboratory environment.

Benefits

• Competitive annual salary commensurate with experience.
• Comprehensive medical and retirement benefits package.
• Paid training and opportunities for professional growth within the QA/QC department.
• Generous annual leave allowance.
• A stable and secure working environment with a focus on quality and compliance.
• Employee assistance program providing confidential support.