Location: Hyderabad, India
Join Lonza’s Global Capability Center (GCC) in Hyderabad and play a key role in global regulatory submissions. As a Specialist in Regulatory Affairs (CMC), you will be responsible for site and customer CMC writing actvities for clinical trial application and product lifecycle support.
What you will get
An agile career and dynamic working culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Opportunities to collaborate with global cross-functional teams. Ongoing learning and professional development opportunities. Our full list of global benefits can be found here: . What you will do
Support the site and customer related regulatory dossier activities for clinical trial applications. Write CMC regulatory dossiers using source documents, ensuring accuracy, completeness, and compliance. S...