Regulatory Affairs Jobs at Genpact | Life Science Graduates | Apply Now
Are you looking for Regulatory Affairs Jobs in top global companies? Here’s an exciting opportunity with Genpact Careers for Life Science graduates! If you’re aiming to build a strong career in Life Science Jobs and want to work in a fast-growing, tech-driven environment, this role could be your perfect next step.
About the Company:
Genpact is a global professional services firm focused on delivering digital transformation through data, technology, and AI. With a strong presence in life science jobs and also in jobs related to regulatory affairs, Genpact helps leading enterprises innovate, optimize operations, and stay competitive in a rapidly evolving world.
Responsibilities:
- The 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 Regulatory Affairs execution.
- Publishing and performing technical validation of eCTD for US submissions.
- Performing final technical quality review, which is a key part of regulatory affairs jobs in this sector.
- 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 acknowledgment from the authority of submission receipt, capturing and the electronic receipt and metadata in RIM, and communicating submission receipt to key stakeholders involved in Regulatory Affairs processes.
- Capturing submissions-related correspondence from health authorities, such as uploading documentation, commitments, and metadata, is essential for regulatory affairs functionality.
Qualifications:
- Bachelor’s degree, preferably in Pharmacy, Medicine, Chemistry, or a related Life science discipline, required with relevant experience in the pharmaceutical industry for regulatory affairs jobs.
- Mandatory Knowledge of ICH and FDA guidelines for the US market, relevant for regulatory affairs roles.
- Working knowledge of eCTD/ CTD/NEES types of submission, industry standard publishing systems needed by candidates pursuing regulatory affairs.
- Should have an advanced level in the English language to excel in regulatory affairs roles at Genpact.
- In-depth working knowledge of eCTD/CTD/NEES/Paper types of submission, industry standard publishing systems is necessary for regulatory affairs.
- Effective time management and organizational skills are highly valued in regulatory affairs jobs.
- Effective communication is crucial for those working in regulatory affairs.
- Flexibility to adapt to a changing environment is key for success in regulatory affairs jobs at Genpact.
Preferred Qualifications/Skills:
- Enthusiasm & confidence will help you in regulatory affairs.
- Adhere to our principles and values, which are important in regulatory affairs roles.
- Time Management skills also support your progress in regulatory affairs jobs careers.
Start your journey with Genpact Careers today and unlock exciting opportunities in Regulatory Affairs Jobs and Life Science Jobs—apply now and take the next big step in your career!
