QC Analyst

Overview

The QC Analyst will execute laboratory testing and quality control activities within a GMP-regulated pharmaceutical manufacturing environment. The role ensures accurate analytical testing, proper sample management, equipment support, and full compliance with cGxP and data integrity standards.

Key Responsibilities

• Perform analytical testing of API, drug substance, drug product, finished product, stability and packaging material samples
• Manage sample storage, handling, and documentation
• Ensure accurate and timely GMP-compliant documentation
• Support equipment maintenance, calibration, and qualification activities
• Maintain inspection readiness and adhere to SOPs, GMP, and HSE standards
• Participate in training, retraining, and continuous improvement initiatives
  
  Requirements & Qualifications

Experience

• Prior experience in pharmaceutical QC laboratory environment
• Hands-on analytical testing experience
• Exposure to GMP documentation and data integrity practices
• Aseptic technique experience

Education

• Diploma / Apprenticeship as Laboratory Assistant or equivalent technical qualification

Technical Knowledge

• QC testing and sampling
• Knowledge of GMP/GxP standards
• Familiarity with laboratory equipment and quality systems

Skills & Competencies

• Detail-oriented and compliance-driven
• Strong documentation discipline
• Team-oriented and result-focused
• Able to work 12-hour rotating shifts