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Regulatory Affairs Specialist

Lonza

Hyderabad, Telangana, India Full-time June 01, 2026
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Opportunity Description

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.
  • Support product ...
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