BPharm Job Vacancy at Accenture | Apply Now for the Regulatory Svs Analyst Role
Accenture is hiring a LifeScience Regulatory Services Analyst for its Hyderabad operations. This BPharm Job requires a Bachelor of Pharmacy and 3 to 5 years of experience in Regulatory Operations. The successful candidate will manage global electronic submissions, including CMC and Life Cycle Management filings, while ensuring adherence to international Health Authority guidelines.
- Job Position: LifeScience Regulatory Svs Analyst
- Location: Hyderabad
- Job ID: AIOC-S01626336
About The Company
Accenture is a global professional services leader with approximately 784,000 employees serving clients across 120 countries. Within its Life Sciences R&D vertical, the company partners with world-leading biopharma companies to improve patient outcomes through clinical, pharmacovigilance, and regulatory innovations. Furthermore, if you are searching for a rewarding BPharm Job, Accenture utilizes advanced digital, cloud, and AI-powered tools to accelerate drug development and regulatory approval cycles.
Role Summary
You will be part of the Clinical, Pharmacovigilance & Regulatory sub-offering, focusing on helping organizations comply with global laws and regulations. It is important to note that for this position, having BPharm Job experience and managing the documentation and resources required for electronic submissions (eCTD) will be essential, ensuring biopharma products meet all legal obligations efficiently.
Key Responsibilities
1. Regulatory Operations & Submissions
- Global Filings: Coordinate the essential documentation and resources required for filing global applications. If your background matches the requirements of the BPharm Job profile, you’ll excel in global filings.
- Electronic Submissions: Process complex electronic submissions, including original filings and Life Cycle Management tasks such as CMC, Ad-promos, amendments, and annual reports.
- SPL Submissions: Manage Structured Product Labeling (SPL) submissions according to defined Health Authority schedules.
2. Documentation & Compliance
- Guidance & Prep: Provide expert guidance on regulatory requirements and prepare necessary technical documentation. In a BPharm Job such as this, technical documentation expertise is crucial for guidance and preparation.
- Compliance Audits: Conduct internal compliance audits to ensure the organization meets all legal standards.
- Technical Readiness: Perform regulatory operations tasks such as bookmarking and hyperlinking granular components of submissions in accordance with ICH guidelines.
3. Strategic Analysis & Interaction
- Problem Solving: Analyze and solve lower-complexity problems, acting as an individual contributor within a focused team, which is often expected in a BPharm Job setting.
- Team Collaboration: Interact daily with peers within Accenture; this role primarily reports to a direct supervisor with limited client exposure.
- Quality Commitment: Maintain a high commitment to quality and accuracy across all regulatory deliverables.
Candidate Requirements
| Category | Requirement |
| Education | Bachelor of Pharmacy (B.Pharm) |
| Experience | 3 to 5 years in Life Sciences Regulatory Operations |
| Skills | Regulatory Services, Regulatory Information Management (RIM) |
| Traits | Adaptable, flexible, team-oriented, and detail-driven |
| Availability | Ability to work in rotational shifts as required |
Why Join Accenture Hyderabad?
- Global Impact: Work with the largest network of Advanced Technology and Intelligent Operations centers to support global biopharma innovators. Obtaining a BPharm Job at Accenture Hyderabad enables you to contribute to global impact in pharmaceutical operations.
- Digital Innovation: Gain exposure to next-gen operating models and digital transformation tools in R&D.
- Inclusive Culture: Join a workplace recognized for its commitment to diversity and equal employment opportunities regardless of background.
