Jr. Research Associate at Vantive
Plymouth, MN 55441, USA -
Full Time


Start Date

Immediate

Expiry Date

09 Nov, 25

Salary

80000.0

Posted On

09 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

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.

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Responsibilities

YOUR ROLE:

This role is aligned within the Vantive kidney care Solutions and Containers R&D Team reporting to the Sr. R&D Manager, Drug Products – Americas Solutions and Containers Team in the USA. As part of the Sustaining Product Organization team you will play a key role in defining, organizing, planning, and leading global multi-functional projects related to all the modalities of Kidney care (PD, HD and Acute). You will also work on new product development projects and innovative technologies supporting improving our products, therapies, and patient outcomes.
This position will work on projects mainly associated with Peritoneal Dialysis (PD) solution and container products and will be responsible for life cycle management.

WHAT YOU WILL BE DOING:

  • Define, organize, plan, and execute activities related to product design change and new product registration in compliance with current international/regional/national regulations with the support of senior colleagues and team members
  • Perform functional testing of dialysis solutions and container products in the laboratory
  • Develop and validate new functional and analytical test methods for polymer materials
  • Provide execution support for product changes related to design, labeling, raw material, manufacturing support, regulatory compliance, quality improvement and new registrations in collaboration with senior scientists
  • Establish, maintain, and update laboratory data, technical reports, & design documentation according to Good Documentation Practices
  • Propose options and develop action plan for problem-solving, product, and process improvement
  • Coordinate and ensure follow-up of technical activities in collaboration with customers, partners, and team members, with respect to project dedication, quality procedures, and business needs
  • Participate in multi-functional and international project team for effective collaboration and deliverables
  • Ensure good internal and cross-functional communication and regular status update of activities
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