Start Date
Immediate
Expiry Date
17 May, 25
Salary
0.0
Posted On
18 Feb, 25
Experience
0 year(s) or above
Remote Job
No
Telecommute
No
Sponsor Visa
No
Skills
Technology, Regulatory Submissions, Biologics, Cmc Regulatory Affairs, Small Molecules, Professional Services
Industry
Pharmaceuticals
GENPACT (NYSE: G) IS A GLOBAL PROFESSIONAL SERVICES AND SOLUTIONS FIRM DELIVERING OUTCOMES THAT SHAPE THE FUTURE. OUR 125,000+ PEOPLE ACROSS 30+ COUNTRIES ARE DRIVEN BY OUR INNATE CURIOSITY, ENTREPRENEURIAL AGILITY, AND DESIRE TO CREATE LASTING VALUE FOR CLIENTS. POWERED BY OUR PURPOSE – THE RELENTLESS PURSUIT OF A WORLD THAT WORKS BETTER FOR PEOPLE – WE SERVE AND TRANSFORM LEADING ENTERPRISES, INCLUDING THE FORTUNE GLOBAL 500, WITH OUR DEEP BUSINESS AND INDUSTRY KNOWLEDGE, DIGITAL OPERATIONS SERVICES, AND EXPERTISE IN DATA, TECHNOLOGY, AND AI.
Inviting applications for the role of Lead Associate CMC Regulatory affairs – Management Trainee - English – On Site Munchen!
This project is staff support to a large client, filling in as a member for their team in-leu of their own. This program is intended to support client in their requested requirement for regulatory submissions that may have impact on registrations of small molecules, biologics and combination products.
GENERAL TASKS:
§ Support and coordination of audit and inspection related activities
§ Maintain up-to-date knowledge of regulatory requirements and guidelines
§ Provide regular progress reports and updates
§ Acting and living in client roles, processes, and systems