Quality Control Analyst - Pharmaceutical

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

Benefits offered by this job

Annual bonuses

Medical aid

Retirement fund contributions

Hybrid work arrangement

Job summary

Placements24 is seeking a detail-oriented Quality Control Analyst for a pharmaceutical manufacturing facility in George. You will ensure quality and safety of products through rigorous testing and analysis within a dedicated QA team.

The role requires 3+ years in QC labs, a chemistry or pharmaceutical science degree, and strong GMP/GLP knowledge. Hybrid work arrangement and opportunities to contribute to patient well-being are offered.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Science, or a related field.
• Minimum of 3 years of experience in a pharmaceutical quality control laboratory.
• Solid understanding of GMP/GLP and regulatory guidelines.

Responsibilities

• Perform routine and non-routine testing of materials and products using analytical techniques (HPLC, GC, UV-Vis).
• Calibrate and maintain laboratory equipment for accuracy and readiness.
• Document testing procedures and results per GLP and GMP standards.
• Investigate out-of-specification results, identify root causes and implement corrective actions.
• Prepare certificates of analysis and other quality documents for product release.
• Support internal and external audits to ensure regulatory compliance.

Skills

Analytical instrumentation

Attention to detail

Multitasking

Education

Bachelor's degree in Chemistry or Pharmaceutical Science

Tools

QC instruments

Job description

About the Role

Our client is seeking a detail-oriented Quality Control Analyst to join their pharmaceutical manufacturing facility in George . This role is essential for ensuring the quality and safety of our pharmaceutical products through rigorous testing and analysis. You will work within a dedicated quality assurance team, upholding the highest standards of compliance with regulatory requirements. The successful candidate will be meticulous, possess strong analytical skills, and be committed to maintaining the integrity of our product lines. This position offers a chance to contribute to patient well-being by ensuring product excellence in a supportive team environment.

Key Responsibilities

• Perform routine and non-routine testing of raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis).
• Calibrate and maintain laboratory equipment, ensuring operational readiness and accuracy.
• Document all testing procedures and results accurately and in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Investigate out-of-specification (OOS) results, identify root causes, and implement corrective actions.
• Prepare certificates of analysis (CoA) and other quality documentation for product release.
• Participate in internal and external audits as required, ensuring regulatory compliance.

Requirements

• Bachelor's degree in Chemistry, Pharmaceutical Science, or a related field.
• Minimum of 3 years of experience in a pharmaceutical quality control laboratory.
• Proficiency with analytical instrumentation commonly used in QC labs.
• Solid understanding of GMP, GLP, and regulatory guidelines relevant to the pharmaceutical industry.
• Excellent attention to detail, organizational skills, and ability to manage multiple tasks effectively.

Benefits

• Competitive salary and potential for annual bonuses.
• Comprehensive medical aid and retirement fund contributions.
• On‑site training and development opportunities.
• Hybrid work arrangement allowing for a balance between office and remote work.
• Be part of a team dedicated to producing high-quality medicines in George .