QC Senior Analyst (m/f/o)

Tasks

• Perform analyses using industry-standard techniques such as HPLC, GC, Spectrophotometry, Dissolution, and Microbiological testing
  
  
• Ensure that all testing is performed according to established analytical methods, SOPs, and regulatory requirements, and that all data are recorded accurately in compliance with Good Documentation Practices (GDP)
  
  
• Conduct and monitor stability studies to evaluate product shelf life and performance under various storage conditions
  
  
• Collaborate with cross-functional teams to support investigations, root cause analysis, and implementation of CAPAs
  
  
• Carry out sampling of raw materials, intermediates, and finished pharmaceutical products in accordance with approved procedures
  
  
• Maintain compliance with Good Laboratory Practice (GLP) and Health & Safety protocols to ensure a safe, efficient, and reliable laboratory environment

Requirements

• A degree in Chemistry, Pharmaceutical Sciences, Microbiology or a related scientific discipline
  
  
• Experience in a pharmaceutical QC laboratory, preferably within a GMP-regulated environment
  
  
• Proven competence in analytical techniques such as HPLC, GC, and Spectroscopy, or Microbiological analysis
  
  
• Strong attention to detail, excellent problem-solving abilities, and the capability to work effectively under pressure
  
  
• Good communication skills in English, both verbally and in writing