Research Associate III – Product Design & Renal Solutions
Location: Bengaluru, Karnataka, India
Category: General R&D / Life Sciences
Employment Type: Full-Time | On-Site
Experience Required: 8–11+ years
About Vantive
Vantive is a pioneering vital organ therapy company dedicated to extending lives and expanding possibilities for patients and care teams worldwide. With over 70 years of leadership in kidney care, Vantive continues to innovate through digital solutions, advanced therapies, and medical devices. Our mission is to provide care teams with greater efficiency and flexibility in therapy administration while helping patients lead longer, fuller lives.
At Vantive, employees join a high-performance, patient-focused community driven by excellence and innovation. Here, your contributions directly impact global healthcare outcomes and advance our legacy of meaningful kidney and vital organ care solutions.
Role Overview
As Research Associate III – Product Design Owner, you will serve as the global technical representative for renal therapy product lines. You will define, plan, and execute product design changes and new registrations, ensuring compliance with international, regional, and national regulations. You will collaborate with senior scientists and cross-functional stakeholders to support product development, lifecycle management, regulatory submissions, and quality improvement initiatives.
Key Responsibilities
Serve as the global Product Design Owner for assigned product lines, including peritoneal dialysis (PD), hemodialysis (HD), and continuous renal replacement therapy (CRRT) products.
Provide technical strategy and assessment for product changes related to design, labeling, raw materials, manufacturing, regulatory compliance, and quality improvement.
Coordinate and monitor technical activities, ensuring alignment with project commitments, quality standards, and business priorities.
Respond to regulatory authority queries in a timely and accurate manner.
Develop action plans and implement solutions for product and process improvements.
Maintain and update Design Control and technical documentation in accordance with Good Documentation Practices (GDP).
Act as a single point of contact for Change Control Board (CCB) activities and metrics within the global renal solutions team.
Participate in multi-functional, international project teams and ensure effective internal and cross-functional communication.
Qualifications & Experience
Master’s in Chemistry or M. Pharm with 11+ years of relevant experience, or Ph.D. in a relevant scientific discipline with 8+ years of relevant experience.
Strong exposure to renal therapies (PD/HD/CRRT), medical devices, and drug products.
Comprehensive understanding of product development stages, lifecycle management, and regulatory requirements.
Demonstrated project/program leadership in pharmaceutical or medical device product portfolios.
Knowledge of Design Control documentation, process improvement, and risk management.
Excellent English verbal and written communication skills.
Ability to manage multiple projects simultaneously and adapt priorities efficiently.
Proficiency in Microsoft Office, WebEx, Teams, and collaboration/documentation tools.
Skills & Competencies
Strong technical and regulatory expertise in drug and device products.
Ability to work independently while collaborating effectively with internal and external stakeholders.
Strong analytical, problem-solving, and decision-making skills.
Flexibility to shift between projects while maintaining delivery timelines.
Understanding of international and regional regulations and global submission requirements.
Portfolio management skills and business acumen for renal PD product lines.
Why Join Vantive
This role offers the opportunity to lead global product design initiatives, influencing renal therapy solutions that improve patient outcomes. You will work on cutting-edge medical devices and drug products, collaborating with global teams while contributing to Vantive’s mission of extending lives and transforming vital organ care.
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