Accenture hiring Life Science Regulatory Services Associate in Bengaluru for BPharm MPharm professionals with Veeva and DocuBridge experience.
Company Overview
Accenture is a globally recognized professional services organization with strong expertise in digital transformation, technology, operations, and regulatory solutions. Serving clients across more than 120 countries, Accenture supports leading life sciences, pharmaceutical, and biotechnology companies in managing complex regulatory, clinical, and compliance requirements. Accenture Hiring Life Science Regulatory
Within its Life Sciences R&D vertical, Accenture delivers end-to-end services covering clinical operations, pharmacovigilance, regulatory affairs, and patient-focused solutions. The organization combines regulatory expertise with advanced technology platforms to help global biopharma companies meet evolving regulatory expectations efficiently and accurately.
To support its growing regulatory operations team, Accenture is hiring skilled professionals for the role of Life Science Regulatory Services Associate in Bengaluru. Accenture Hiring Life Science Regulatory
Job Location & Employment Type
- Job Location: Bengaluru, Karnataka (BDC9A)
- Employment Type: Full-time
- Work Mode: Office-based
- Department: Regulatory Services – Life Sciences
- Job Schedule: Rotational shifts may apply
Open Positions / Department Details
- Position Title: Life Science Regulatory Services Associate
- Skill Category: Regulatory Services – Life Sciences Regulatory Operations
- Job Requisition ID: AIOC-S01624477
- Functional Area: Clinical, Pharmacovigilance & Regulatory Services
This role focuses on regulatory operations and electronic submission support for global pharmaceutical and life sciences clients.
Key Roles & Responsibilities
As a Life Science Regulatory Services Associate, the selected candidate will support regulatory submission and compliance activities. Key responsibilities include: Accenture Hiring Life Science Regulatory
- Coordinating regulatory documentation and resources required for global regulatory submissions
- Supporting preparation and processing of electronic submissions for original filings and lifecycle management activities
- Handling submissions related to:
- CMC documentation
- Amendments and variations
- Annual reports
- SPL submissions
- Promotional and advertising materials
- Working with regulatory publishing tools to manage submission packages
- Ensuring regulatory documents meet submission standards and authority expectations
- Supporting compliance with global regulatory requirements and timelines
- Solving routine regulatory and operational issues using established guidelines and procedures
- Working closely with team members and reporting progress to direct supervisors
- Following detailed instructions for daily tasks and new assignments
- Maintaining accuracy, quality, and traceability of regulatory documentation
- Contributing as an individual team member within a defined scope of work
Eligibility Criteria
Education
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
Candidates with formal education in pharmacy and regulatory-related subjects will be preferred.
Experience
- 1 to 3 years of relevant experience in regulatory operations or regulatory publishing
Skills Required
- Mandatory hands-on experience with:
- Veeva Vault
- DocuBridge publishing tools
- Understanding of regulatory submission processes and lifecycle management
- Familiarity with global regulatory frameworks and documentation standards
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Ability to follow structured workflows and compliance-driven processes
- Strong attention to detail and documentation accuracy
- Good communication and collaboration skills
- Willingness to work in rotational shifts if required
Accenture Hiring Life Science Regulatory
Salary & Benefits
- Salary: As per Accenture company norms
Additional benefits may include:
- Opportunity to work with global life sciences clients
- Exposure to large-scale regulatory operations and digital publishing platforms
- Structured learning and career development programs
- Inclusive and diverse workplace culture
- Long-term growth opportunities within Accenture’s life sciences practice
Accenture Hiring Life Science Regulatory
Selection Process
The selection process may include:
- Resume screening based on regulatory operations experience
- Technical interview focusing on regulatory publishing tools and processes
- HR discussion and final selection
The exact process may vary based on project and business requirements. Accenture Hiring Life Science Regulatory
How to Apply
- Mode of Application: Online Application Only
Interested candidates should apply through the official Accenture careers portal using the job requisition ID mentioned above. No walk-in or email applications are specified for this role. Accenture Hiring Life Science Regulatory
Important Dates
- Last Date to Apply: Not specified (apply at the earliest)
Why Apply for This Pharma Job?
This role is ideal for regulatory professionals looking to strengthen their expertise in global regulatory operations and electronic submissions. Working at Accenture provides exposure to advanced regulatory publishing tools, international regulatory requirements, and large-scale life sciences projects, making it a strong career move for pharmacy graduates with regulatory experience.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent pharmaceutical and life sciences job information platform and is not affiliated with Accenture or any organization mentioned. All job details are shared strictly for informational purposes. Candidates should verify information and apply only through official company channels. Accenture Hiring Life Science Regulatory
Final Call-to-Action
If you have regulatory operations experience and hands-on skills in Veeva and DocuBridge, apply now to grow your career with a global life sciences services leader. Accenture Hiring Life Science Regulatory
