Not specified; not specified; competitive salary +...
Liquid chromatography (lc) method development
Lc-uv/ms detection expertise
Method validation experience
The role involves developing reliable chromatographic test methods for analyzing active pharmaceutical ingredients and their related impurities
Job Summary
The role involves developing reliable chromatographic test methods for analyzing active pharmaceutical ingredients and their related impurities.
Candidates will join the Analytical Method & Stability Center to support drug development by combining strong analytical science with end-to-end stability expertise.
The position offers the opportunity to work in a dynamic, international team dedicated to making a difference in healthcare innovation.
Matching Summary
The role involves developing reliable chromatographic test methods for analyzing active pharmaceutical ingredients and their related impurities.
Salary
Not specified; Not specified; Competitive salary and excellent benefits mentioned
Skills & Requirements
Must-have
Liquid Chromatography (LC) method development
LC-UV/MS detection expertise
Method validation experience
Stability testing execution
Project management skills
Nice-to-have
Digital enabled technology platforms
Peptide and conjugate synthesis knowledge
Agile working environment adaptability
Proactive attitude towards innovation
Collaboration across analytical teams
Key Requirements
PhD in Analytical Chemistry or related field with 3+ years experience
Master's degree in chemistry with 7+ years experience
In-depth expertise in LC-UV/MS method development and validation