Life Sciences Regulatory Affairs Associate at Accenture Bengaluru
A rare chance has emerged for aspiring Life Sciences professionals through Accenture Regulatory Affairs Jobs, including this Regulatory Affairs Associate opening in Bengaluru. This role is suitable for candidates with 1 to 3 years of experience in regulatory operations and eCTD publishing, holding an M.Pharm qualification. Interested individuals are encouraged to apply promptly.
About the Company
Accenture is a global professional services company with leading capabilities in digital, cloud, and security. The organization combines unmatched experience and specialized skills across more than 40 industries, offering Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. With a workforce of approximately 784,000 people, Accenture serves clients in more than 120 countries, embracing the power of change to create value and shared success for clients, people, shareholders, partners, and communities.
- Company: Accenture
- Location: Bengaluru, BDC9A, India
- Experience: 1 to 3 years
- Qualification: M.Pharm
- Posted On: 28 August 2026
- Employment Type: Full-time
- Hiring Organization: Accenture Solutions Pvt Ltd
Accenture Regulatory Affairs Jobs: Job Description
The Life Sciences Regulatory Affairs Associate, an Accenture regulatory affairs role for experienced M.Pharm professionals, will be responsible for performing regulatory operations tasks, including bookmarking and hyperlinking submission documents in accordance with ICH guidelines and other health authorities. The incumbent will also conduct quality control checks for all submission components, collect and evaluate scientific data from R&D, and ensure compliance with current regulations.
Key Responsibilities
- Work on end-to-end planning, coordination, compilation, publishing, and dispatch of global regulatory lifecycle submissions across multiple health authorities.
- Ensure regulatory dossiers and submission packages comply with regional requirements, eCTD standards, and applicable regulatory guidelines.
- Manage submission timelines, lifecycle activities, renewals, variations, supplements, annual reports, and post-approval regulatory changes.
- Collaborate with cross-functional stakeholders to track submission readiness, resolve gaps, and support timely health authority interactions and responses.
- Utilize Regulatory Information Management Systems (RIMS), publishing tools, and quality review processes to deliver compliant, high-quality submissions with on-time execution.
Eligibility Criteria
- Master of Pharmacy (M.Pharm)
- 1 to 3 years of relevant experience in regulatory affairs.
How to Apply
Interested candidates can apply for the position through the following link:
Conclusion
This position at Accenture presents a significant opportunity for qualified candidates seeking Accenture Regulatory Affairs Jobs to advance their careers in Life Sciences Regulatory Affairs. Interested individuals are encouraged to apply before the deadline to secure their chance to contribute to a leading global professional services company.
