Pharmaceutical Quality Control Analyst - Centurion

Placements24; Centurion; On-site; ZAR 420,000 - 660,000; Full time

Benefits offered by this job

Health insurance

Retirement fund contributions

Professional development

Job summary

Placements24 is seeking a meticulous Pharmaceutical Quality Control Analyst for our client’s facility in Centurion, Gauteng. The role focuses on analytical testing of raw materials, in-process samples, and finished products, using HPLC, GC, UV-Vis, and dissolution apparatus within a GMP/GLP framework.

You will document results, investigate OOS events, and participate in method validation and CAPA activities while maintaining safety and quality across all QC operations.

Qualifications

• BSc in Chemistry, Analytical Chemistry, Pharmacy or related field.
• 2–3 years of experience in a pharma QC lab.
• Hands-on HPLC and GC experience is essential.
• Familiarity with GLP and GMP practices.

Responsibilities

• Perform analytical testing of raw materials, in-process samples, and finished products according to approved specs and methods.
• Operate and maintain HPLC, GC, UV-Vis spectrophotometers, and dissolution equipment.
• Document all activities, results, and deviations per GMP guidelines.
• Investigate OOS results and implement CAPAs.
• Contribute to method validation and transfers.
• Maintain laboratory cleanliness and safety compliance.
• Assist in QC reports and summaries.
• Support continuous improvement initiatives and regulatory compliance.

Skills

Analytical chemistry

GLP

GMP

Teamwork

Documentation

Education

BSc in Chemistry/Analytical Chemistry/Pharmacy

Tools

HPLC

GC

Job description

About the Role

Our client, a leading pharmaceutical manufacturer, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their facility in Centurion, Gauteng . This role is critical to ensuring the quality, safety, and efficacy of our pharmaceutical products through rigorous testing and analysis. You will perform a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory equipment. The ideal candidate will have a strong foundation in analytical chemistry, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP). This is an excellent opportunity for a dedicated professional to contribute to a reputable company committed to upholding the highest standards in pharmaceutical manufacturing. You will work closely with the quality assurance team to ensure compliance with all regulatory requirements and internal quality standards.

Key Responsibilities

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products according to approved specifications and test methods.
• Operate and maintain a range of laboratory instruments, including HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Prepare reagents, solutions, and standards required for analytical testing.
• Document all laboratory activities, test results, and deviations accurately and promptly in accordance with GMP guidelines.
• Investigate out-of-specification (OOS) results and implement corrective and preventive actions (CAPAs).
• Participate in method validation and transfer activities.
• Maintain laboratory cleanliness and ensure adherence to safety protocols.
• Assist in the preparation of quality control reports and summaries.
• Contribute to continuous improvement initiatives within the quality control laboratory.
• Stay current with pharmacopeial standards (e.g., USP, BP, EP) and relevant regulatory guidelines.

Requirements

• Bachelor of Science degree in Chemistry, Analytical Chemistry, Pharmacy, or a related scientific discipline.
• Minimum of 2-3 years of experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with HPLC and GC is essential; experience with other analytical techniques is a plus.
• Proficiency in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Strong understanding of analytical chemistry principles and methodologies.
• Excellent documentation and record-keeping skills.
• Ability to work independently and as part of a team in a fast-paced environment.
• Strong problem-solving and critical thinking abilities.
• Good organizational and time management skills.
• Familiarity with South African pharmaceutical regulations.

Benefits

Our client offers a competitive salary, comprehensive health insurance, retirement fund contributions, and opportunities for professional development and training. You will work in a state-of-the-art facility with a commitment to employee growth and well-being. This role provides the chance to contribute to the production of life-saving medicines and to be part of a company that values quality and integrity above all else. We offer a stable and supportive work environment where your expertise will be recognized and rewarded. Join our dedicated team in Centurion and advance your career in pharmaceutical quality control.