This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Summary

As R&D Renal Chronic Disposables Engineer you’ll be responsible for the  Risk Management process of a product family of disposables for hemodialysis and manage design projects within the same family of products.

The candidate will work in a dynamic R&D team. The team is taking in charge the development of disposables for Hemodialysis treatments and own the products DHF and manage it along the products shelf life.

The candidate will be required to follow the risk management process of a product category according to the corporate Baxter procedure and will be required to issue technical protocols and reports that will be part of the Design History File of the product's portfolio managed by the team.

Essential duties and responsibilities

• Manage the risk management files of a product family maintaining and revising them on a regular base
• Follow the execution of design project activities assuring the highest quality and design products standard.
• Prepare and review Protocol Plans and Reports for the qualification of materials, components and finished products as far as their pre-clinical evaluation is concerned, and with the support of Subject Matter Experts plan and redact the most appropriate testing strategy for the physical evaluation of material, components and finished devices.
• Manage, plan and support relevant testing activities
• Prepare working and operative instruction pertaining to the matter of competence, with reference to the frame of V&V activities

What you’ll bring

• Master Degree in scientific disciplines
• 2 years of experience in the medical device or pharma industry, preferably in R&D
• Knowledge of European and US Medical device regulation
• Good knowledge of English (written and spoken)
• Good communication skills; ability to work in team and independently

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to [email protected] and let us know the nature of your request along with your contact information.

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