Quality Control Analyst - Pharmaceutical Raw Materials

Placements24; Klerksdorp; Presencial; ZAR 350.000 - 520.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical aid and retirement fund

Generous annual leave

On-site parking

Descripción de la vacante

Placements24 in Klerksdorp is seeking a meticulous Quality Control Analyst to join our pharmaceutical client’s team. The role focuses on analytical testing of raw materials and finished products, ensuring quality and regulatory compliance in a GMP/GDP environment.

You will perform HPLC, GC, UV-Vis and other analyses, document results accurately, support method validation, and assist during internal audits and regulator inspections.

Formación

• Bachelor of Science in Chemistry, Biochemistry, Pharmacy or related life science discipline.
• Minimum of 3 years as a QC Analyst in pharmaceutical industry, focused on raw material testing.
• Strong experience with analytical techniques (HPLC, GC, UV-Vis, IR spectroscopy) and wet chemistry methods.
• Knowledge of GMP, GLP and pharmacopeial standards (USP/EP/BP).

Responsabilidades

• Perform analytical tests on incoming raw materials, intermediates, and finished products.
• Document testing procedures and results in accordance with GLP and GMP.
• Investigate out-of-specification (OOS) results and participate in root-cause investigations.
• Review and approve analytical data for raw materials and components.
• Maintain a clean, safe laboratory and assist in internal audits and regulator inspections.

Conocimientos

HPLC

GC

UV-Vis

IR spectroscopy

Wet chemistry

Educación

Bachelor of Science in Chemistry/Biochemistry/Pharmacy

Herramientas

LIMS

Descripción del empleo

About the Role

Our client, a prominent pharmaceutical manufacturer, has an immediate opening for a meticulous Quality Control Analyst to join their dedicated team in Klerksdorp . This role is critical to ensuring the quality and integrity of all raw materials used in the production of life-saving medications. You will perform a variety of analytical tests, meticulously documenting results and adhering to strict quality control protocols and regulatory guidelines. This is a laboratory-based position requiring hands-on analytical expertise and a deep commitment to upholding the highest standards of pharmaceutical quality. Become an essential part of the quality assurance framework at our Klerksdorp facility.

Key Responsibilities

• Perform a range of analytical tests on incoming raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, spectroscopy, titration).
• Prepare reagents, standards, and samples for analysis according to established methods.
• Operate and maintain laboratory equipment, ensuring proper calibration and functionality.
• Document all testing procedures and results accurately and thoroughly in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Investigate out-of-specification (OOS) results, identify root causes, and participate in corrective action investigations.
• Review and approve analytical data and documentation for raw materials and components.
• Ensure compliance with all relevant regulatory requirements (e.g., FDA, SAHPRA) and internal SOPs.
• Contribute to method validation and transfer activities as required.
• Maintain a clean, safe, and organized laboratory environment.
• Participate in internal audits and provide support during external regulatory inspections.

Requirements

• Bachelor of Science degree in Chemistry, Biochemistry, Pharmacy, or a related life science discipline.
• Minimum of 3 years of experience as a QC Analyst in the pharmaceutical industry, with a focus on raw material testing.
• Strong practical experience with analytical techniques such as HPLC, GC, UV-Vis, IR spectroscopy, and wet chemistry methods.
• Proficiency in laboratory documentation, data review, and understanding of pharmacopeial standards (e.g., USP, EP, BP).
• Knowledge of GMP, GLP, and relevant regulatory guidelines.
• Excellent attention to detail and accuracy in performing tests and recording data.
• Good organizational and time management skills.
• Ability to work independently and as part of a collaborative team in our Klerksdorp laboratory.
• Effective problem-solving skills related to analytical testing.
• Familiarity with laboratory information management systems (LIMS) is a plus.

Benefits

• Competitive salary package commensurate with experience and qualifications.
• Comprehensive medical aid and retirement fund options.
• Generous annual leave and holiday allowances.
• Opportunities for further training and professional development in pharmaceutical analysis.
• Access to modern analytical instrumentation and laboratory facilities.
• A stable and secure working environment within a reputable company.
• Contribution to ensuring the quality and safety of pharmaceutical products.
• Supportive team culture and management.
• Potential for career progression within the Quality Unit.
• On-site parking and convenient location in Klerksdorp .