LifeScience Regulatory Services Associate Job at Accenture
Launch your life sciences regulatory career with Accenture in Bengaluru. This Associate Job full-time LifeScience Regulatory Services Associate role offers the opportunity to work with global biopharma clients, supporting regulatory submissions, document quality checks, and compliance processes. Perfect for fresh graduates and early-career pharmacy professionals eager to build expertise in regulatory operations within a world-leading professional services organization. Graduates searching for b pharm freshers job or M Pharm jobs can apply.
Introduction of the Job
Accenture is hiring a LifeScience Regulatory Services Associate to support regulatory operations, submissions, document QC, and compliance processes in alignment with global standards.
Associate Job Details
- Support regulatory document processing, bookmarking, and hyperlinking
- Review and transform source regulatory documents
- Perform quality control checks for submission components
- Manage electronic submissions including CMC, amendments, SPL, annual reports
- Coordinate required documents for global submission filings
- Work within Life Sciences R&D vertical supporting clinical, PV & regulatory functions
- Work may require rotational shifts
About the Company
Accenture is hiring a LifeScience Regulatory Services Associate in Bengaluru for candidates with Bachelor or Master of Pharmacy qualifications and 0-2 years of experience. The role supports regulatory operations, including electronic submissions, document review, bookmarking, hyperlinking, and quality control aligned with ICH and global authority requirements. You will work within the Life Sciences R&D vertical supporting clinical, regulatory, and pharmacovigilance operations. This role offers hands-on experience in global regulatory submissions, compliance documentation, and electronic filing for leading biopharma companies, while working alongside industry experts in a high-performance, technology-driven environment.
Educational Requirements for Associate Job Role:
- Bachelor of Pharmacy (B.Pharm) or
- Master of Pharmacy (M.Pharm)
- Experience: 0-2 years (1-3 years mentioned acceptable as per job note)
Key Responsibilities for Associate Job Role:
- Execute regulatory operations tasks and electronic submissions
- Conduct document quality checks (QC) and compliance reviews
- Follow ICH and global regulatory guidelines
- Assist in life cycle management filings for biopharma clients
- Follow structured processes with detailed instructions
Skills Required for Associate Job Role:
- Quick learning ability
- Adaptability & flexibility
- Problem-solving mindset
- Ability to work under pressure
- Strong commitment to quality
- Team collaboration & communication skills
How to Apply for Associate Job Role:
Graduates searching for b pharm freshers job or M Pharm jobs can apply through Accenture’s official careers portal by uploading your resume and completing the online application form.
