Stability Analyst

• Performing sample and batch analysis using HPLC, GC, and other analytical techniques
• Preparing, labelling, and managing samples in line with SOPs
• Generating, analysing, and reporting data in compliance with GMP/GLP standards
• Monitoring trends and identifying any out-of-specification or unexpected results
• Supporting stability study protocols and data interpretation
• Contributing to method development, validation, and transfer activities
• Participating in lab investigations, CAPA processes, and audit readiness
• Ensuring compliance with health & safety, quality systems, and regulatory requirements
• Driving continuous improvement initiatives across the laboratory

• Degree in a relevant scientific discipline (e.g. Chemistry, Pharmaceutical or Biological Science) or equivalent experience
• Hands-on experience with analytical techniques such as HPLC (desirable)
• Experience within healthcare, FMCG, or medical device environments is advantageous
• Strong attention to detail with a quality-focused mindset
• Self-motivated, proactive, and able to manage workload effectively
• Excellent communication and interpersonal skills

Hands-on experience with analytical techniques such as HPLC

• Comprehensive technical and GMP training
• Opportunities to gain exposure to method development, validation, and advanced lab processes
• A strong focus on continuous improvement and professional development
• The chance to work with a globally recognised client in a collaborative environment