Junior Research Associate

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

Essential Duties & Responsibilities

• As Tech Lead or Change Owner, define, organize, plan, and execute activities related to product design change, supplier related changes, new product registration and strategic or value improvement projects compliance with current international/regional/national regulations with support from senior colleagues as and when necessary.
• Propose, formulate, and coordinate action plans for implementation of changes and related activities by working closely with PDO Organization, Project Management, Regulatory, Quality, senior colleagues, and the other cross-functions.
• Expected to develop, document, test and manage product related changes in accordance with established Kidney Care product processes and stay aligned with Quality Management System. Ensure good internal and cross-functional communication and regular status update of activities.
• Establish, maintain, and update technical & Design documentation according to Good Documentation Practices. Propose, participate, or lead ideation sessions for product enhancement and exploratory activities to foster innovation culture within team.
• Assist in providing technical support to queries from MOH authorities or auditors (internal/external) in due time by collaborating with cross-functions and subject matter experts.
• Ensure Quality & Compliance to Vantive policy/Ethics/Data Integrity.
• Assist in preparing formulation development plan and execute formulation lab activities/trials as per the design of experiment with good documentation practices.

Qualification

• Master’s degree in science or pharmaceutical disciplines is required.
• Good technical depth & knowledge of scientific disciplines Agile and flexible to work in a regulated environment.
• Critical thinker and good communication with ability to articulate the project status and summary.

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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