Regulatory Affairs Specialist Hiring at Vantive

Regulatory Affairs Specialist Hiring at Vantive

Join Vantive – A Leader in Kidney Care and Vital Organ Therapy

Are you a skilled Regulatory Affairs Specialist looking for a career in the healthcare industry? Vantive, a global leader in kidney care and organ therapy, is hiring Regulatory Affairs Specialists in Bengaluru, Karnataka. This role offers an exciting opportunity to work on regulatory documentation, compliance, and submissions for drug, device, and combination products.

Why Join Vantive?

Vantive has been at the forefront of kidney care innovations for over 70 years. With a strong commitment to digital solutions and advanced therapies, the company provides a dynamic and growth-oriented work environment. This is your chance to impact lives while advancing your career in regulatory affairs.

Job Overview

• Position: Regulatory Affairs Specialist
• Job Category: Regulatory Affairs
• Location: Bengaluru, Karnataka, India
• Job Reference: JR – 179406

Key Responsibilities

• This role resides within the Regulatory Operations – Systems and Submissions Operations organization. This function will partner with Global IT (GIT) and Global Regulatory Affairs (GRA)/Global Business Units (GBU) on the following:
  • Management of Veeva RIMVault, PromoMats, CCDS, and other systems
  • Processing license requests for Drug and Medical Devices in Veeva RIMVault system
  • Supporting Data Governance of Veeva RIMVault system (Regulatory Information Management System) and PromoMats
  • CCDS Coordination between Central CCDS team and Country Affiliates (to make sure timely submission of CCDS Updates to HA and CCDS Tracking Tool updates)
  • Experience in accessing and retrieving documentation from electronic document management systems
  • Will have to work independently with minimal support.
  • Will be co-located with the current Regulatory Operations team in Bengaluru, India a minimum of 3 days per week.
  • Will work with global regulatory leads (GRLs) across the Globe for Drugs and Devices
  • Verify the maintenance of support systems, libraries, and dictionaries

Required Qualifications

• M-Pharm (Pharmaceutics)
• 4-6 years’ experience in Regulatory Affairs expertise, highly proficient in supporting and maintenance of Regulatory Information Management Systems (deep Veeva RIMVault and Veeva PromoMats) and other regulatory systems.

Preferred Skills

• Strong project management and organizational abilities.
• Excellent interpersonal and communication skills.
• Ability to work in a fast-paced, regulated environment.

How to Apply?

Interested candidates can apply now by visiting the official Vantive careers page. Don’t miss this opportunity to work with a leader in kidney care and regulatory compliance!

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