Job Title: Life Sciences Regulatory Services Analyst
Job ID: AIOC-S01620286
Location: Bengaluru, Karnataka, India
Job Type: Full-Time
Experience Required: 3–5 Years
Industry: Life Sciences | Regulatory Affairs | Regulatory Operations
Accenture is a global professional services leader with strong capabilities in digital, cloud, and security. With expertise across more than 40 industries, Accenture delivers Strategy & Consulting, Technology, Operations, and Accenture Song services through the world’s largest network of Advanced Technology and Intelligent Operations centers. With a workforce of over 699,000 professionals across 120+ countries, Accenture helps organizations drive innovation and achieve sustainable growth through technology and human ingenuity.
Accenture is hiring a Life Sciences Regulatory Services Analyst to support regulatory operations within its Life Sciences R&D vertical. This role focuses on regulatory compliance, global submissions, and lifecycle management activities, supporting leading biopharmaceutical companies in meeting global regulatory requirements efficiently and accurately.
The position is well-suited for professionals with hands-on experience in regulatory operations, electronic submissions, and regulatory documentation within the pharmaceutical or life sciences domain.
Support regulatory services by ensuring compliance with global regulatory requirements and internal quality standards
Coordinate documentation and resources required for global regulatory submissions
Prepare, manage, and process electronic submissions including:
Original application filings
Lifecycle Management submissions (CMC variations, amendments, annual reports)
Advertising and promotional submissions
Structured Product Labeling (SPL) submissions
Monitor and stay updated on evolving regulatory guidelines and compliance requirements
Assist in regulatory audits and compliance reviews as required
Perform analysis and resolution of low to medium complexity regulatory issues
Collaborate primarily with internal peers and supervisors, with limited client interaction
Work as an individual contributor within a structured team environment
Adhere to defined timelines, SOPs, and quality benchmarks
Support operations that may require working in rotational shifts
3–5 years of experience in Life Sciences Regulatory Operations or Regulatory Services
Working knowledge of global regulatory submission processes and lifecycle management
Experience handling electronic submission platforms and regulatory documentation
Strong understanding of regulatory compliance, documentation standards, and quality processes
Ability to follow structured work instructions and manage multiple tasks efficiently
Good analytical, organizational, and communication skills
Bachelor of Pharmacy (B.Pharm)
Candidates with relevant regulatory affairs or life sciences regulatory operations experience will be preferred
Individual contributor role with defined scope of work
Moderate supervision with detailed guidance for new assignments
Decisions primarily impact individual deliverables and team outcomes
Work with global life sciences and biopharma clients
Gain exposure to end-to-end regulatory operations and compliance activities
Be part of a globally recognized organization with strong learning and career growth opportunities
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