Quality Experts

Description

• Independently plan and perform analytical studies, including method development, verification, validation, and transfer.
• Implement and optimize new analytical techniques and support stability studies and other analytical support activities.
• Interpret, document, and report analytical results to provide timely, high-quality support to quality control, production, and development.
• Own and manage all analytical documentation (analytical plans, sampling plans, specifications).
• Ensure equipment qualification and effective management of reference standards.
• Drive technological improvements and process optimization, including the upgrade and transfer of expertise within quality control.
• Execute complex quality- and compliance-relevant activities in line with internal regulations, good practices, legislation, and regulatory/Novartis requirements.
• Contribute to risk management, inspection readiness, quality management activities, and end-to-end management of internal and external quality-related projects.

Qualifications

• University degree in pharmacy, chemistry, biology, microbiology, veterinary medicine, or another relevant natural or engineering science.
• PhD in a relevant discipline preferred, especially for senior/expert roles.
• Solid experience in analytical methods (development, validation, transfer) within a regulated environment (e.g., pharma, biotech).
• Strong understanding of GxP, regulatory expectations, and quality systems.
• Proven ability to interpret complex analytical data and produce clear, structured reports.
• Experience with equipment qualification and management of analytical reference standards.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Fluent in English (written and spoken); additional languages are an advantage.