Looking for Regulatory Affairs jobs in Bengaluru? Here’s an excellent opportunity for pharmacy professionals. Accenture is hiring LifeScience Regulatory Services Associates for its Life Sciences Regulatory Operations team in Bengaluru. Candidates with B.Pharm or M.Pharm qualifications and 1โ3 years of experience can apply for this full-time opportunity.
This role is ideal for professionals interested in Regulatory Affairs, eCTD submissions, Life Cycle Management (LCM), CMC documentation, regulatory compliance, and global pharmaceutical regulatory operations. Working with Accenture provides exposure to leading global biopharmaceutical clients while building expertise in regulatory services.
Job Highlights
| Particular | Details |
|---|---|
| Company | Accenture |
| Position | LifeScience Regulatory Services Associate |
| Department | Regulatory Services โ Life Sciences Regulatory Operations |
| Job Location | Bengaluru, Karnataka |
| Employment Type | Full-Time |
| Qualification | Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm) |
| Experience | 1โ3 Years |
| Shift | Rotational Shifts |
| Job ID | AIOC-S01659392 |
About Accenture
Accenture is one of the world’s leading professional services organizations providing services across consulting, technology, cloud, operations, AI, and digital transformation. The company works with healthcare and pharmaceutical organizations worldwide to accelerate innovation across research, clinical development, regulatory affairs, pharmacovigilance, and patient services.
Key Responsibilities
As a LifeScience Regulatory Services Associate, you will:
- Coordinate documentation required for global regulatory submissions.
- Support preparation and management of electronic regulatory submissions.
- Process original application filings and regulatory documentation.
- Handle Life Cycle Management (LCM) activities.
- Support CMC submission documentation.
- Prepare amendments and annual reports.
- Process SPL (Structured Product Labeling) submissions.
- Ensure compliance with global regulatory requirements.
- Maintain accurate regulatory documentation.
- Work with internal teams to complete submission timelines.
- Follow established regulatory procedures and quality standards.
- Resolve routine operational issues using defined guidelines.
- Meet submission deadlines while maintaining accuracy.
Required Qualifications
Candidates should possess:
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
Experience Required
- 1โ3 years of experience in Regulatory Affairs or Regulatory Operations.
Desired Skills
Applicants should have:
- Regulatory Affairs knowledge
- Regulatory Operations experience
- Electronic Submission Management
- eCTD submission understanding
- Life Cycle Management (LCM)
- CMC documentation experience
- Regulatory compliance knowledge
- Excellent communication skills
- Stakeholder management
- Client relationship management
- Ability to handle multiple priorities
- Time management
- Adaptability and flexibility
Preferred Technical Knowledge
Experience in any of the following will be beneficial:
- Electronic regulatory submissions
- Global regulatory filings
- CMC documentation
- Product lifecycle submissions
- Annual reports
- Amendments
- SPL submissions
- Regulatory document management
Why Join Accenture?
Working with Accenture offers:
- Opportunity to work with global pharmaceutical companies.
- Exposure to international regulatory affairs projects.
- Career growth in Life Sciences Regulatory Operations.
- Collaborative work environment.
- Learning and professional development.
- Experience with global regulatory submission processes.
- Stable career with a leading multinational organization.
Salary
Based on similar Regulatory Operations Associate roles in Bengaluru, the expected salary range is:
โน4.8 LPA โ โน7.2 LPA (Approximate, depending on skills and experience).
How to Apply
