Pharmaceutical Quality Control Analyst

Placements24; Gqeberha; On-site; ZAR 420,000 - 620,000; Full time

Benefits offered by this job

Medical aid

Provident fund

Competitive salary

Job summary

Placements24 in Port Elizabeth is seeking a meticulous Pharmaceutical Quality Control Analyst to ensure the safety and quality of medicines in a busy GMP-regulated laboratory.

You will perform a range of analytical tests on raw materials, in-process samples, and finished products, operate instruments like HPLC, GC, and UV-Vis, and document results in accordance with GMP/GLP standards. This role offers stability in a growing pharmaceutical environment in the Eastern Cape.

Qualifications

• Bachelor’s degree in Chemistry or related field with regulatory exposure.
• 2–3 years’ experience as QC Analyst in pharma or regulated sector.
• Strong GMP/GLP knowledge and pharmacopeial standards familiarity.

Responsibilities

• Perform quantitative and qualitative analysis of raw materials, intermediates, and finished products using validated methods.
• Document laboratory activities accurately per GMP/GLP and maintain records.
• Analyze test results, report deviations, and support investigations of OOS results.
• Assist in method validation, transfer activities, and keep equipment in good condition.

Skills

Analytical chemistry

Data interpretation

Teamwork

Attention to detail

Education

Bachelor's degree in Chemistry or Analytical Chemistry or Pharmacy

Tools

HPLC

GC

FTIR

UV-Vis

Dissolution apparatus

Job description

About the Role

Our client, a reputable pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their operations in **Port Elizabeth, Eastern Cape**. In this crucial role, you will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet predefined quality specifications and regulatory standards. Your work will directly contribute to the safety and efficacy of the medicines produced. The ideal candidate will have a strong foundation in analytical chemistry and experience with various laboratory techniques and instrumentation. This position offers a stable and secure career path within a growing organization located in the industrial hub of **Port Elizabeth**. You will work within a well-equipped laboratory, contributing to the overall quality assurance framework of the company in **Eastern Cape**.

Key Responsibilities

• Perform quantitative and qualitative analysis of raw materials, intermediates, and finished products using validated analytical methods.
• Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
• Document all laboratory activities accurately and comprehensively in compliance with GMP and GLP.
• Analyze test results, compare them against specifications, and report any deviations or out-of-specification (OOS) results.
• Prepare reagents, standards, and solutions required for testing.
• Participate in method validation and transfer activities.
• Ensure compliance with all safety procedures and maintain a clean and organized laboratory environment.
• Contribute to the investigation of OOS results and deviations.
• Assist in the maintenance of laboratory records and inventory of supplies.

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline.
• Minimum of 2-3 years of experience as a QC Analyst in the pharmaceutical or a related regulated industry.
• Proficiency in using analytical instruments like HPLC, GC, FTIR, UV-Vis, and dissolution apparatus.
• Strong understanding of GMP, GLP, and pharmacopeial standards (e.g., USP, BP, EP).
• Excellent laboratory technique, data interpretation, and documentation skills.
• Good problem-solving abilities and attention to detail.
• Ability to work independently and as part of a team in a fast-paced environment.
• Effective written and verbal communication skills.
• Experience with LIMS (Laboratory Information Management System) is advantageous.

Benefits

Our client offers a competitive annual salary, a comprehensive medical aid plan, and a provident fund. You will have the opportunity to work with modern analytical instrumentation and receive ongoing training to enhance your skills. This role is based in **Port Elizabeth**, providing a stable employment opportunity within the **Eastern Cape**. Our client fosters a supportive team environment and values the contribution of each team member to product quality and patient safety. Secure your career in pharmaceutical quality control.