Quality Control Analyst - Pharmaceutical Testing

Placements24; Bellville; Hybrid; ZAR 420,000 - 660,000; Full time

Benefits offered by this job

Competitive salary

Medical aid

Retirement fund

Training opportunities

Modern laboratory facilities

Parking

Job summary

Placements24 is seeking a detail-oriented Quality Control Analyst to join a pharmaceutical client in Centurion, Gauteng. The role covers qualitative and quantitative testing of raw materials, in‑process samples, and finished products to ensure GMP/GLP compliance and pharmacopeial standards.

You will use HPLC, GC, UV-Vis, FTIR, and dissolution methods, maintain data in LIMS, and assist with method validation and investigations.

Qualifications

• Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences or related field.
• Minimum of 3 years of experience in a pharmaceutical QC lab.
• Hands-on with HPLC and GC; knowledge of GMP/GLP and regulatory guidelines.

Responsibilities

• Perform qualitative and quantitative analytical tests on raw materials, intermediates, and finished products using HPLC, GC, UV-Vis, FTIR and dissolution testing.
• Prepare reagents, standards, and samples for analysis following established procedures.
• Document results accurately in laboratory notebooks and electronic systems (LIMS).
• Calibrate, maintain, and troubleshoot laboratory instruments to ensure performance and compliance.
• Review and interpret data, report deviations to supervisors, and participate in method validation/transfer activities.

Skills

Analytical thinking

Problem solving

Detail oriented

Communication

Teamwork

Education

Bachelor's degree in Chemistry or related field

Tools

HPLC

GC

LIMS

UV-Vis

FTIR

Job description

About the Role

Our client, a prominent player in the pharmaceutical industry, is seeking a detail-oriented and experienced Quality Control Analyst to join their dedicated team in Centurion, Gauteng. This crucial role involves performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent quality and regulatory standards. The successful candidate will be proficient in various analytical techniques and possess a thorough understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). This is an excellent opportunity to contribute to the safety and efficacy of medicines within a supportive and scientifically driven environment. You will work with sophisticated laboratory equipment and collaborate with other QC personnel, QA professionals, and production staff. We are looking for an individual with strong analytical skills, a commitment to accuracy, and a proactive approach to identifying and resolving quality issues. This position is essential for maintaining our client's reputation for producing high-quality pharmaceutical products.

Key Responsibilities

• Perform qualitative and quantitative analytical tests on raw materials, intermediates, and finished products using various techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Prepare reagents, standards, and samples for analysis according to established procedures.
• Document all test results accurately and meticulously in laboratory notebooks and electronic systems.
• Calibrate, maintain, and troubleshoot laboratory instruments to ensure optimal performance and compliance.
• Review and interpret analytical data, identifying any deviations from specifications and reporting them to supervisors.
• Participate in method validation and transfer activities for new analytical procedures.
• Ensure compliance with all relevant regulatory requirements, including GMP, GLP, and pharmacopeial standards (e.g., USP, EP).
• Maintain laboratory cleanliness and ensure proper disposal of chemical waste.
• Assist in the investigation of out-of-specification (OOS) results and customer complaints.
• Contribute to continuous improvement initiatives within the Quality Control department.

Requirements

• Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum of 3 years of experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with HPLC and GC is essential; experience with other compendial methods is a strong asset.
• Knowledge of GMP, GLP, and relevant regulatory guidelines.
• Proficiency in using laboratory information management systems (LIMS).
• Strong analytical, problem-solving, and organizational skills.
• Excellent attention to detail and accuracy in data recording and reporting.
• Ability to work effectively both independently and as part of a team.
• Good understanding of statistical analysis relevant to QC testing.
• Effective written and verbal communication skills.

Benefits

• Competitive annual salary and potential for performance-based incentives.
• Comprehensive medical aid and retirement fund benefits.
• Generous annual leave entitlement.
• Opportunities for professional development and further training in analytical techniques.
• Access to modern laboratory facilities and advanced analytical instrumentation.
• A collaborative team environment with experienced colleagues.
• Contribution to the development and release of essential medicines.
• Employee wellness programs.
• Company-provided uniform and safety equipment.
• Parking available at the facility.