Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Lifescience Regulatory Svs Specialist

Accenture
7-11 years
INR 14 LPA – 25 LPA
Bangalore, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines

LifeScience Regulatory Services Specialist (Team Lead / Consultant)

Company: Accenture
Job ID: AIOC-S01649533
Location: Bengaluru
Employment Type: Full Time
Department: Regulatory Services – Life Sciences Regulatory Operations
Qualification: B.Pharm / M.Pharm
Experience: 7–11 Years
Language: English (Professional Proficiency)


About the Role

Accenture is looking for an experienced Regulatory Operations professional to support global regulatory submissions and lifecycle management activities within its Life Sciences R&D division. The role focuses on coordinating regulatory documentation, managing electronic submissions, supporting global product registrations, and ensuring compliance with regulatory requirements across multiple markets.

This position combines Regulatory Affairs Operations, submission management, stakeholder coordination, and team leadership responsibilities.


Key Responsibilities

  • Coordinate global regulatory submission activities.

  • Prepare and manage documentation required for regulatory filings.

  • Support original application submissions and product registrations.

  • Handle Life Cycle Management (LCM) submissions.

  • Manage CMC variations, amendments, annual reports, and promotional submissions.

  • Process electronic submissions using regulatory publishing systems.

  • Ensure regulatory documentation complies with global requirements.

  • Support regulatory compliance audits and inspections.

  • Collaborate with cross-functional global teams and regulatory stakeholders.

  • Analyze operational challenges and implement process improvements.

  • Lead small teams or workstreams while ensuring project timelines are met.

  • Support regulatory operations activities across different markets.


Core Areas of Work

  • Regulatory Operations

  • Electronic Submissions (eCTD)

  • Regulatory Publishing

  • Life Cycle Management (LCM)

  • CMC Submission Support

  • Annual Reports

  • Amendments & Variations

  • SPL Submissions

  • Global Product Registrations

  • Regulatory Documentation Management


Required Skills

  • Regulatory Affairs Operations

  • Global Submission Management

  • eCTD Publishing

  • Regulatory Documentation

  • CMC Knowledge

  • Regulatory Compliance

  • Stakeholder Management

  • Project Coordination

  • Team Leadership

  • Problem Solving & Analysis

  • Communication Skills


Preferred Experience

  • 7–11 years in Regulatory Operations or Regulatory Affairs.

  • Experience with global submissions (FDA, EMA, MHRA, Health Canada, etc.).

  • Knowledge of eCTD publishing tools and submission software.

  • Experience with lifecycle management submissions.

  • Familiarity with Veeva Vault RIM, Documentum, or similar regulatory systems.

  • Prior experience managing small teams or client-facing projects.