Research Associate III (PDO)
Location: Bengaluru, India
Job ID: JR - 179675
Job Type: Full-time
Department: Research and Development
Date Posted: July 22, 2025
Estimated Salary: ₹16 – ₹25 LPA (based on qualifications and experience)
About Vantive:
Vantive is a leader in vital organ therapy, transforming patient care through innovation in kidney care and beyond. For over 70 years, we’ve delivered pioneering solutions, and today, we’re expanding access through digital tools, cutting-edge science, and a commitment to longer, fuller lives. At Vantive, your work has purpose, your voice matters, and your growth is limitless.
Role Overview:
As a Research Associate III (PDO), you will lead solution development for parenteral drug products, managing both new product development and lifecycle activities. You will serve as the technical lead, overseeing design control, product specifications, regulatory support, and cross-functional coordination on a global scale.
Key Responsibilities:
Technical Leadership:
Act as Solution Lead and technical expert for drug product R&D projects.
Provide mentoring and guidance to execution scientists to meet milestones.
Ensure alignment with QA, environmental, and regulatory standards.
Product Development & Lifecycle Management:
Plan and execute formulation and product changes, supplier transitions, and labeling.
Review and approve Design Control documentation per industry standards.
Maintain and update product specifications and associated verification/validation records.
Risk and Regulatory Support:
Collaborate with Product Risk Owners for risk analysis linked to design changes.
Support regulatory submissions and global product launches.
Respond to authority queries and provide technical justifications.
Stakeholder & Resource Management:
Estimate and forecast resources for projects.
Facilitate effective communication across global, cross-functional teams.
Provide regular project updates to stakeholders and leadership.
Qualifications:
Education:
Master’s in Chemistry or M.Pharm. with 10–12 years of relevant experience
OR Ph.D. in Pharmaceutical or relevant science with 7–10 years of experience in parenteral solution development
Required Skills:
Strong background in parenteral formulation development and lifecycle management
Familiarity with medical devices and combination products
Expertise in Design Control, GMP, and ICH guidelines
Experience with Product Risk Management and regulatory submissions
Proven project/program leadership and stakeholder management skills
Proficiency in technical documentation and cross-border communication
Ability to work independently and drive vision at a strategic level
Why Join Vantive?
Lead development for life-sustaining therapies
Work at the intersection of science, innovation, and patient care
Collaborate in a diverse, global team that values courage, focus, and excellence
Shape the future of drug-device combination therapies in a mission-driven organization
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