Qa Non-Conformity Technician Medolla

Qa Non-Conformity Technician
Medolla
Emilia Romagna, Medolla

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 for a QA Non-Conformity Technician to join our Quality Assurance team in Medolla (MO).

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.

This position as QA Non-Conformity Technician at Baxter is a great opportunity to develop your professional career in a very challenging Quality area regulated by international standards such as FDA 21CFR820 or ISO 13485.

**What you'll be doing

- Make activities related to complaints and non-conformities technical investigation in order to find the root cause of events according to applicable procedures;

- Verify that all information, including samples returned from the field or scrapped 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;

- Supports trend investigations through the review of manufacturing batch records, evaluation of returned product, product reserve sample inspections, and review of complaint histories and trends;

- Recommends disposition of all involved product to the Quality Unit.

**What you'll bring

- Preferable Degree in Engineering (biomedical, electronical, chemical ) or Technical Diploma in Biomedical Field

- Previous experience in Quality areas 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 in English.

**Reasonable Accommodations

**Recruitment Fraud Notice

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To learn how you can protect yourself, review our Recruitment Fraud Notice.

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