We're sorry, the job you are looking for at Lonza on EuroPharmaJobs has expired.
Click here to see more jobs at Lonza .
We still have many live jobs. Click below for similar jobs in:
or go to our job search page.
You will be responsible for leading cross-functional regulatory CMC activities to ensure timely preparation and delivery of high-quality regulatory submissions that support product development, registration, and lifecycle management. This position
Lead the development of new chemical entities with a focus on Drug Substance matters. Lead manufacturing and scale-up activities toward API including supplies of building blocks, Regulatory starting materials or GMP intermediates