genpact
A Specialist in Regulatory Affairs Strategy at Genpact executes validation and quality reviews for eCTD submissions to US health authorities. The role involves coordinating submission dispatches, managing post-submission correspondence, and maintaining metadata within Risk Information Management systems within a highly regulated pharmaceutical environment.
Headquarters
New York, New York, United States
Company Size
10001+ employees
Founded
1997
Genpact is an agentic and advanced technology solutions company that uses process intelligence and AI to deliver measurable outcomes for businesses. It enables digital transformation through intelligent automation, analytics, and process optimization across industries. With a global delivery network and deep domain expertise, Genpact partners with enterprises to reimagine operations, improve efficiency, and accelerate value from data-driven insights. The company emphasizes practical, ROI-focused technology solutions that blend AI, automation, and process excellence to drive tangible business results.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for genpact.
genpact didn’t post a salary, so this is our estimate from similar listings.
27% below the average for this role
Regulatory Affairs Specialist
kymanox
Regulatory Affairs Specialist
Jackson Healthcare
Senior Associate, Regulatory Affairs CMC
Iovance Biotherapeutics
Manager, Regulatory Affairs
BeOne Medicines
Executive, Regulatory Operations (eCTD Publishing)
oraclecloudinfrastructure
Regulatory Affairs Associate
Integrated Resources INC