Regulatory Affairs Jobs at Genpact | BSc Chemistry Graduates Apply Now
Are you looking for high-impact Regulatory Affairs Jobs in the pharmaceutical industry? Genpact Careers offers an exciting opportunity for a Lead Associate – Regulatory Affairs in Mumbai. This role is perfect for professionals with a background in Pharmacy, Life Sciences, or BSc Chemistry Jobs, who want to work on global regulatory submissions, eCTD publishing, and FDA-compliant operations. Join a dynamic team driving compliance and innovation across global pharma operations.
About Genpact
Genpact is a global technology and services company delivering transformative solutions to leading enterprises worldwide. With expertise in AI, digital, and operational excellence, Genpact provides professionals with opportunities to work on cutting-edge projects across industries, including pharmaceuticals. By joining Genpact Careers, candidates can explore impactful Regulatory Affairs Jobs, BSc Chemistry Jobs, and contribute to global pharmaceutical compliance while advancing their careers in a dynamic and innovative environment.
Details
- Job Post: Lead Associate – Regulatory Affairs(LIF022816)
- Location: Mumbai, India
Job Purpose
The Lead Associate – Regulatory Affairs will manage global regulatory operations, ensuring submissions comply with ICH and FDA guidelines. This includes handling eCTD, CTD, NeeS, and paper submissions for the US market. The role requires technical validation, quality review, and post-submission processing, supporting cross-functional teams across Cipla sites. This position is ideal for candidates pursuing Regulatory Affairs Jobs, Genpact Careers, or BSc Chemistry Jobs seeking exposure to global pharmaceutical compliance.
Key Responsibilities
- Publish and validate eCTD submissions for US regulatory authorities.
- Conduct final technical quality review and dispatch submissions to relevant authorities or affiliates.
- Capture submission-related correspondence, documentation, and metadata in RIM.
- Support APQR, CPV, and stability activities with statistical and regulatory insights.
- Ensure compliance with ICH, FDA, and global regulatory standards.
- Provide guidance and internal training on submission processes, publishing tools, and regulatory requirements.
Qualifications and Skills
- Bachelor’s degree in Pharmacy, Life Sciences, Chemistry, or related discipline. BSc Chemistry Jobs candidates with regulatory experience are encouraged to apply.
- Strong knowledge of ICH guidelines, CTD structure, and US FDA submissions.
- Expertise with publishing tools like Liquent, DocuBridge, and eCTD platforms.
- Excellent English communication, time management, and organizational skills.
- Ability to adapt to a fast-paced, regulated environment.
Why join Genpact?
Joining Genpact as a Lead Associate – Regulatory Affairs offers an unmatched opportunity to advance your career in Regulatory Affairs Jobs while working on global pharmaceutical submissions and compliance projects. You will gain hands-on experience with eCTD, CTD, and FDA regulatory operations, collaborating with cross-functional teams across geographies. Genpact provides a culture of continuous learning, mentorship, and innovation, making it ideal for professionals pursuing BSc Chemistry Jobs or broader pharmaceutical career growth. By joining Genpact Careers, you become part of a dynamic, values-driven organization that empowers you to shape the future of pharma regulatory operations while accelerating your personal and professional development.
