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Lead Associate - Regulatory Affairs-Lif022816

Genpact
Genpact
3-5 years
Not Disclosed
10 Dec. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Lead Associate – Regulatory Affairs Operations (Global)
Location: Mumbai, India
Job Type: Full-time
Experience Required: 3–5 years in Regulatory Affairs or Pharmaceutical Industry
Education: Bachelor’s degree in Pharmacy, Medicine, Chemistry, or Life Sciences

Company Overview:
Genpact is a global leader in advanced technology services, delivering AI, automation, and digital solutions to help enterprises transform at scale. With a strong focus on innovation, operational excellence, and data-driven solutions, Genpact empowers companies across industries to work smarter, grow faster, and solve complex challenges. Join over 140,000 professionals who thrive in a dynamic, tech-driven, and values-oriented culture. Learn more at genpact.com.

Role Overview:
The Lead Associate – Regulatory Affairs will manage global regulatory submissions and ensure compliance with ICH, FDA, and regional guidelines. This role involves publishing, validating, and dispatching eCTD/CTD/NEES/Paper submissions, tracking correspondence with health authorities, and supporting the regulatory operations team in a fast-paced, process-driven environment.

Key Responsibilities:

  • Publish and perform technical validation of eCTD submissions for US and global markets.

  • Conduct final technical quality reviews prior to submission.

  • Dispatch submissions to regulatory authorities or affiliates for further processing.

  • Perform post-submission activities including acknowledgement tracking, metadata capture in Regulatory Information Management (RIM) systems, and stakeholder communication.

  • Manage submission-related correspondence from health authorities, including uploading documentation, commitments, and metadata.

  • Collaborate with cross-functional teams to ensure timely and accurate regulatory submissions.

Required Qualifications & Skills:

  • Bachelor’s degree in Pharmacy, Medicine, Chemistry, or related Life Sciences discipline.

  • Strong knowledge of ICH guidelines, FDA regulations, and US market requirements.

  • Proficiency in eCTD/CTD/NEES submissions and industry-standard publishing systems such as Liquent, DocuBridge, or similar.

  • Advanced English language skills (written and verbal).

  • Excellent organizational, time management, and communication skills.

  • Ability to adapt to a dynamic and changing regulatory environment.

Preferred Qualifications:

  • 3–5 years of experience in regulatory operations or pharmaceutical regulatory affairs.

  • Experience with global submission processes and cross-functional collaboration.

  • Strong attention to detail, flexibility, and problem-solving capability.

Why Join Genpact:

  • Lead innovation at the forefront of AI, automation, and digital transformation.

  • Drive meaningful impact by solving real-world regulatory and business challenges.

  • Access continuous learning, mentorship, and career advancement opportunities.

  • Collaborate with global teams and work on high-visibility regulatory projects.

  • Thrive in a culture rooted in courage, curiosity, integrity, and inclusion.

Equal Opportunity Statement:
Genpact is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, sex, age, national origin, disability, sexual orientation, gender identity, veteran status, or any other legally protected status. Genpact does not charge fees for recruitment or hiring. Candidates should report any fraudulent activity to the company immediately.