Lead Business Analyst – RIMS / Regulatory Affairs at Vueverse

💼 Now Hiring: Lead Business Analyst – RIMS / Regulatory Affairs at Vueverse 💼

📍 Location: India (Remote/Hybrid as per company norms)
🗂️ Industry: Pharmaceuticals / Life Sciences

Vueverse is looking for a dynamic and experienced Regulatory Business Analyst to lead digital transformation initiatives in Regulatory Information Management (RIM) using Veeva Vault. If you're passionate about streamlining regulatory operations and have hands-on experience with regulatory systems, this role is crafted for you!

🔍 Key Responsibilities:

Liaise with Regulatory Affairs and IT teams to translate business needs into system enhancements.

Implement and optimize Veeva Vault RIM modules: Submissions, Registrations, Archive, and Product.

Prepare and manage documentation: BRDs, FRDs, process flows, traceability matrices.

Support data migration, validation, and UAT phases of Veeva Vault RIM.

Recommend improvements in regulatory workflows aligned with FDA, EMA, and ICH standards.


✅ Required Skills:

6+ years as a Business Analyst in Pharma/Life Sciences.

2+ years of hands-on experience in Veeva Vault RIM.

Strong understanding of submission lifecycle, labeling, lifecycle management, and compliance.

Familiarity with eCTD, IDMP, XEVMPD, and GxP.

Excellent communication and stakeholder management skills.


⭐ Preferred (Nice-to-Have):

Experience with ArisGlobal, Lorenz docuBridge, or MasterControl.

Exposure to Agile/Scrum.

Knowledge of Veeva Vault Quality or PromoMats.


👉 Apply now and be part of a cutting-edge regulatory transformation journey in the pharmaceutical industry.


✨How to apply:
Apply here: Application link

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