Analyst IV – Sample Management & Analytical Testing

About the role

The Analyst IV will be responsible for the storage, management and analytical testing of drug product, finished product, stability and packaging material samples in compliance with GxP standards. This position supports the timely reporting of technical complaints and adverse events related to Novartis products.

Key responsibilities

• Store and manage samples, ensuring integrity and traceability.
• Perform analytical testing and document results for drug, finished product, stability and packaging material samples according to GxP guidelines.
• Document stability testing data and maintain compliance with SOPs.
• Report technical complaints, adverse events and special case scenarios within 24 hours of receipt.
• Distribute marketing samples where applicable.
• Support method validation and verification activities.
• Monitor key performance indicators such as order accuracy, lead time, deadline adherence and inspection readiness.

Required profile

• Strong understanding of GMP, GxP and GSU guidelines.
• Ability to work under tight deadlines and report issues promptly.
• Attention to detail and commitment to maintaining documentation quality.
• Experience in a regulated pharmaceutical laboratory environment.

Required skills

• GxP compliance
• GMP knowledge
• Stability testing
• Analytical documentation
• Method validation/verification

What we offer

• Opportunity to work within a leading global pharmaceutical company.
• Exposure to a wide range of analytical techniques and regulatory processes.
• Professional development through a structured training plan.