Regulatory Affairs Professional With Experience In Global Ectd/Ctd/Nees/Actd Submissions (Xico)

Regulatory Affairs Professional With Experience In Global Ectd/Ctd/Nees/Actd Submissions (Xico)

12 sep
|
Genpact
|
Xico

12 sep

Genpact

Xico

Ready to shape the future of work?
At Genpact, we don't just adapt to change—we drive it.
AI and digital innovation are redefining industries, and we're leading the charge.
Genpact's, our industry-first accelerator, is an example of how we're scaling advanced technology solutions to help general enterprises work smarter, grow faster, and transform at scale.
From large-scale models to, our breakthrough solutions tackle companies' most complex challenges.
If you thrive in a fast-moving, tech-driven environment, love solving real-world problems, and want to be part of a team that's shaping the future, this is your moment.
Genpact (NYSE: G) is an advanced technology services and solutions company that delivers lasting value for leading enterprises globally.
Through our deep business knowledge, operational excellence, and cutting-edge solutions – we help companies across industries get ahead and stay ahead.
Powered by curiosity, courage, and innovation,our teams implementdata, technology, and AI to create tomorrow, today.
Get to know us atand on,,, and.Inviting applications for the role of Regulatory Affairs AnalystThe Role demands for a publisher with demonstrated ability to execute responsibility in a highly regulated & process driven environment, the Person will be responsible for all the activities related to.ResponsibilitiesPublishing and performing technical validation of e CTD for US submissions.
Performing final technical quality review.
Dispatching submission to the relevant authority (e CTD/CTD/Nee S/Paper) or affiliate so that affiliate can dispatch to authority.




Performing post-submission processing activities such as receiving acknowledgement from authority of submission receipt; capturing and the electronic receipt and metadata in RIM; communicating submission receipt to key stakeholders.
Capturing submissions-related correspondence from health authorities, such as uploading documentation, commitments and metadata.Qualifications
Minimum QualificationsBachelor's degree, preferably in Pharmacy, Medicine, Chemistry, or related Life science discipline required with relevant experience in the pharmaceutical industry.
Mandatory Knowledge of ICH and FDA guideline for US market.
Working knowledge of e CTD/ CTD/NEES types of submission, industry standard publishing systems.
Should be advance level in English language.
In depth working knowledge of e CTD/CTD/NEES/Paper types of submission, industry standard publishing systems.
Effective time management and organizational skills.
Effective communication.
Flexibility to adapt to a changing environment.Preferred QualificationsEnthusiasm & confidence
Adhere to our principles and values.
Time Management skills.Why join Genpact?
Be a transformation leader– Work at the cutting edge of AI, automation, and digital innovation
Make an impact– Drive change for global enterprises and solve business challenges that matter
Accelerate your career– Get hands-on experience, mentorship, and continuous learning opportunities
Work with the best– Join 140,000+ bold thinkers and problem-solvers who push boundaries every day
Thrive in a values-driven culture– Our courage, curiosity, and incisiveness - built on a foundation of integrity and inclusion - allow your ideas to fuel progress
Come join the tech shapers and growth makers at Genpact and take your career in the only direction that matters: Up.
Let's build tomorrow together.

📌 Regulatory Affairs Professional With Experience In Global Ectd/Ctd/Nees/Actd Submissions (Xico)
🏢 Genpact
📍 Xico

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