Jobs at Accenture | M Pharm Graduates Apply Now For The LifeScience Regulatory Svs Analyst Role
Accenture is hiring a LifeScience Regulatory Services Analyst in Bengaluru for professionals with 3–5 years of experience and a Master of Pharmacy degree. This role offers an opportunity to work in regulatory affairs, ensuring compliance with global health authority requirements while supporting leading biopharma companies. Join Accenture’s Life Sciences R&D vertical to contribute to regulatory submissions, dossier preparation, and compliance strategies in a dynamic environment.
- Job Position: LifeScience Regulatory Svs Analyst
- Location: Bengaluru, India
- Job ID: AIOC-S01600998
About the Company
Accenture is a global professional services company with expertise in digital, cloud, and security. With unmatched experience across more than 40 industries, Accenture delivers Strategy and Consulting, Technology and Operations services, and Accenture Song—powered by one of the world’s largest networks of Advanced Technology and Intelligent Operations centers. With over 775,000 employees serving clients in more than 120 countries, Accenture drives innovation and positive change through technology and human ingenuity.
Job Description
As a LifeScience Regulatory Services Analyst, you will be aligned with Accenture’s Life Sciences R&D vertical. Your role will focus on regulatory affairs, supporting the preparation of dossiers, life cycle management activities, and compliance with ICH and global health authority requirements. You will ensure that all regulatory documentation complies with international standards while contributing to strategies that bring innovative therapies to patients.
Key Responsibilities
- Perform regulatory affairs life cycle management tasks, including dossier building and coordination.
- Review and transform source documents for submissions.
- Conduct Quality Control (QC) checks for all submission components.
- Collect, collate, and evaluate scientific data generated during the research and development (R&D) process.
- Guide scientific constraints and regulatory requirements.
- Ensure organizational products comply with current regulations.
- Build regulatory submission strategies, author regulatory documents, and prepare health authority packages.
- Work with peers and supervisors on problem-solving and project execution.
- Adapt to rotational shifts when required.
Qualifications
- Master of Pharmacy (M.Pharm)
- 3–5 years of relevant experience in regulatory services
- Strong knowledge of life sciences regulatory requirements and Veeva Vault
- Ability to manage multiple stakeholders and meet deadlines
- Team-oriented with agility for quick learning
Keywords: LifeScience Regulatory Services Analyst, Regulatory Services, Life Sciences, Regulatory Affairs, Accenture, Bengaluru, Job Postings.
