QA Ncr Technician

**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**:
A great opportunity has recently arisen in our Quality Assurance Department in Medolla.

The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products.

We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialogue builds trust within the team and helps create a better product for our customers.

The job as QA NCR Technician at Baxter is a great opportunity to develop your professional career in a very challenging Quality area regulated by international standards as FDA 21CFR820 or ISO 13485.

This is a temporary position

**What you'll do**:

- Make activities related to the evaluation and investigation of manufacturing nonconformities in order to find the root cause of events according to applicable procedures;
- Verify that all information, including samples discarded during manufacturing processes, are available to perform investigation activities;
- Perform testing activities necessary to reproduce the alleged failure;
- Define data analyses to support activities;
- Write investigations reports in order to document properly the activities in accordance with good documentation practice (GDP);
- Avoid processes stop, collaborating and guaranteeing speed and effectiveness with an audit proof approach;
- Recommends disposition of all involved products to the Quality Unit.

**Qualifications**:

- Technical Diploma in Biomedical Field or Degree in Engineering (biomedical, electronical, chemical )
- Previous experience in the Quality area in the medical industry is preferred;
- Organization skills and ability to do multiple tasks at once;
- Good communication and interpersonal skills;
- Problem-Solving attitude;
- Fluent knowledge of English.

**Reasonable Accommodations**

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