Job Description

Location: Hyderabad, India
Join Lonza’s Global Capability Center (GCC) in Hyderabad and play a key role in global regulatory submissions. As a Senior Specialist in Regulatory Affairs (CMC), you will lead dossier authoring activities across development and commercial programs.
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.
Support product lifecycle management activities
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Regulatory Affairs Senior Specialist

Job Description

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