Research Scientist I – Kidney Care Solutions
Req #: JR-188825
Location: Whitefield, Bangalore, India
Job Category: General R&D
Employment Type: Full-Time
Company Overview:
Vantive is a pioneering organ therapy company dedicated to extending lives and improving care for patients worldwide. Building on nearly 70 years of expertise in kidney care, Vantive delivers advanced solutions in acute therapies, home and in-center dialysis, and is expanding into broader vital organ therapies. Our mission is to provide innovative, patient-centered solutions while fostering a culture of excellence, courage, and collaboration.
Role Summary:
We are seeking a Research Scientist I to serve as a Product Design Owner (PDO) or PDO Support within its product family for Kidney Care Solutions. This role will provide technical leadership and manage lifecycle development activities, ensuring compliance with international, regional, and national regulations while supporting product innovation, registration, and global deployment.
Key Responsibilities:
Act as technical expert and Product Design Owner (PDO) for assigned product family within R&D Kidney Care Solutions.
Organize, plan, and execute development and sustaining activities in compliance with QA, environmental, and regulatory standards.
Review and approve Design Control documentation, including Design History Files, technical specifications, and validation/verification documents.
Mentor and guide project leads and change owners to meet project milestones and business objectives.
Coordinate product changes, supplier changes, labeling updates, and lifecycle management tasks.
Support global product registration, launch, and regulatory queries.
Provide technical leadership for product/process improvements, cost optimization, and risk management.
Ensure effective communication across internal and cross-functional teams globally, providing regular project status updates.
Contribute to product-related publications, presentations, and innovation initiatives.
Experience & Requirements:
Master’s degree in Chemistry or M.Pharm with minimum 14 years of relevant experience, or PhD in a related discipline with minimum 7 years of relevant experience.
Proven experience in medical devices, drug products, product development, and lifecycle management.
Strong knowledge of Design Control documentation, product risk management, and regulatory compliance (international, regional, national).
Demonstrated project/program leadership and ability to work independently.
Excellent English verbal and written communication skills.
Strong organizational, problem-solving, and documentation skills; ability to manage multiple projects and priorities effectively.
Experience in stakeholder management at a global level.
Why Join Vantive:
Vantive offers the opportunity to work on transformative therapies in a mission-driven environment. You will join a global, collaborative, and innovative team committed to improving patient care while developing your professional expertise.
Equal Employment Opportunity & Accessibility:
Vantive is an equal opportunity employer. We provide reasonable accommodations to qualified individuals with disabilities globally and are committed to fostering an inclusive workplace.
Learn More: Vantive Careers
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