Accenture
Published On: 30 July 2025
Position: Life Science Regulatory Affairs Services Associate
Openings: Single Role
Experience: 0–2 Years
Qualification Required: B.Pharm, M.Pharm
Mode of Application: Online Application via Company Website

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🏢 About Accenture

Accenture is a global professional services giant, operating in over 120 countries with more than 699,000 employees. It excels in digital transformation, cloud, security, and strategy. Accenture's Life Sciences R&D division supports global pharmaceutical clients by streamlining regulatory operations, clinical research, pharmacovigilance, and product lifecycle management, helping speed up market access for essential medicines.

📌 Position: Life Science Regulatory Affairs Services Associate

Key Responsibilities:
✔ Perform regulatory documentation tasks including bookmarking and hyperlinking.
✔ Transform and validate submission documents per ICH, FDA, EMA guidelines.
✔ Conduct Quality Control (QC) of submissions.
✔ Manage eCTD and electronic submissions (original filings, amendments, CMC, SPLs, etc.).
✔ Assist with Life Cycle Management (LCM) documentation.
✔ Support regulatory filings globally in collaboration with international teams.

📍 Location: Bengaluru

✅ Eligibility Criteria

• Qualification: B.Pharm or M.Pharm

• Experience: 0–2 years

• Basic knowledge of regulatory operations, pharmacovigilance, and clinical research preferred.

• Strong attention to detail and ability to handle documentation.

💼 Skills Required

• Familiarity with ICH, FDA, and EMA regulatory guidelines

• Understanding of eCTD submission formats

• QC and documentation handling skills

• Ability to work in a global collaborative environment

📋 Hiring Process

Mode: Online Application Only
Apply via: Accenture Official Careers Page – Click Here

Documents to Prepare:

• Updated Resume

• Educational Certificates

• Valid Government ID

• Work Experience Proof (if any)

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