Regulatory Affairs Jobs at Genpact | BSc Chemistry Graduates Apply Now
Are you looking for rewarding Regulatory Affairs Jobs with a global leader in digital innovation? Genpact is hiring Technical Associates in Regulatory Affairs, offering an excellent opportunity for science graduates to grow their careers in a tech-driven, high-performance environment. This role is perfect for professionals seeking Genpact Careers that combine AI, compliance, and regulatory publishing. Candidates with backgrounds in pharmacy, life sciences, or chemistry will find this an attractive option, especially those exploring Chemistry Jobs in a regulated and rapidly evolving industry.
About Genpact
Genpact is a global leader in advanced technology services and digital transformation, helping enterprises accelerate growth through AI, analytics, and innovation. With deep industry expertise and a strong focus on operational excellence, Genpact partners with Fortune 500 companies to solve complex challenges and build smarter workflows. The company offers exceptional opportunities for professionals exploring Regulatory Affairs Jobs, Genpact Careers, and Chemistry Jobs in a dynamic, future-ready environment. Rooted in values of integrity, curiosity, and inclusiveness, Genpact empowers its teams to shape meaningful change while driving sustainable impact for clients worldwide.
Job Details
- Job: Technical Associate
- Location: India-Mumbai
- Education Level: Bachelor’s / Graduation / Equivalent
Job Overview
Genpact invites applications for the role of Technical Associate – Publisher for the US Market (Regulatory Affairs – Operations). Candidates should be freshers or have minimal experience with good knowledge of ICH guidelines, CTD structures, and publishing tools such as Liquent and DocuBridge.
Responsibilities
- The Role demands 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.
- Publishing and performing technical validation of eCTD for US submissions.
- Performing final technical quality review.
- Dispatching submission to the relevant authority (eCTD/CTD/NeeS/Paper) or affiliate so that the affiliate can dispatch to the authority.
- Performing post-submission processing activities such as receiving acknowledgement from the authority of submission receipt, capturing and the electronic receipt and metadata in RIM, and communicating submission receipt to key stakeholders.
- Capturing submissions-related correspondence from health authorities, such as uploading documentation, commitments, and metadata.
Qualifications
- Bachelor’s degree, preferably in Pharmacy, Medicine, Chemistry, or a related Life science discipline, required with relevant experience in the pharmaceutical industry.
- Mandatory Knowledge of ICH and FDA guidelines for the US market.
- Working knowledge of eCTD/ CTD/NEES types of submission, industry standard publishing systems.
- Should have an advanced level in the English language.
- In-depth working knowledge of eCTD/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.
Why Join Genpact?
Genpact offers an exciting platform for professionals aiming to grow in Regulatory Affairs Jobs, Genpact Careers, and Chemistry Jobs within a globally recognized tech-driven environment. With access to cutting-edge AI, digital tools, and industry-leading platforms like the AI Gigafactory, you’ll work on real-world challenges that shape the future of global operations. Genpact promotes continuous learning, mentorship, and cross-functional exposure, enabling rapid career growth. Its culture of innovation, integrity, and inclusiveness ensures a supportive workplace where your ideas and expertise can thrive. Joining Genpact means being part of a team that drives transformation and creates meaningful impact worldwide.
