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.

We are looking to hire a Quality Engineer (f/m/d) – Technical Service in fulltime for our site in Saalfeld/ Thüringen. 

Our mission is deeply connected to our work!

About Baxter Saalfeld:

Saalfeld's technology and automation are innovative. From Emergency, Surgical, Intensive, and Med-Surge Care, our solutions deliver real-time insights and help care teams deliver phenomenal outcomes!

For surgical teams and nursing staff to work efficiently, increase user comfort, and improve patient safety.

Your Role at Baxter:

This is where your creativity addresses challenges.

You are creative, detailed, and a hands-down doer. You accept a challenge and apply your team's collaborative powers to produce great results. You are motivated by work that is never the same from one day to the next. This role supports the field service activities and service centers in the DACH region regarding quality management and actively participates in the design, implementation, and maintenance of quality processes.

Your Team at Baxter:

Every role within Quality makes a difference. We draw energy from working in a plant or an office where there are opportunities to collaborate. As the company evolves, so does our team's approach to work as it strives to create top-of-the-line products.

What you'll be doing:

Ensuring compliance with quality assurance processes in the front and back office as well as in the field operations and service centers

Ensuring that Global Services processes and procedures align with regulatory requirements, the company's quality manual, and ISO 9001 and ISO 13485 requirements.

Maintaining close relationships with the Global Services team, Quality Technical Service team in EMEA, and other relevant collaborators

Responsibility for documentation, training, internal as well as external audits, CAPA and non-conformances, compliance with post-marketing surveillance activities, supplier qualification, validation processes, change control processes, and risk assessments within own area of responsibility

Support and ensure compliance with field and service center operations related to equipment release, labeling, storage areas, calibration, decontamination, equipment validation, repair, PM, and spare parts management.

Monitor and establish quality critical metrics and initiate actions.

Support and lead local, European, and global projects and initiatives.

What you'll bring:

Completed master's degree in biomedical, electrical/electronic engineering or equivalent degree in technical/technological field.

Several years(ggf. Job starter) of experience in quality management in a medical device company or experience in technical service/manufacturing/R&D environment

Knowledge of quality systems and quality assurance in operations as well as technical service processes

Knowledge of ISO 9001 and ISO 13485 standards

Ability to handle various tasks in an international environment.

Ability to understand and solve technical systems.

Affinity to IT systems and good office skills, especially in the use of MS-Excel

Proficient in German and English, both written and spoken

Willingness to travel

What we offer you:

As an internationally active company, we offer you professional training opportunities and fair remuneration with above-average social benefits, a company pension scheme, a share plan for employees, 30 days vacation plus special leave, and additional insurance is a matter of course, for us.

For further information, please reach out to Mr Sebastian Lange via E-Mail: sebastian_lange@baxter.com

Baxter is committed to supporting the needs for flexibility in the workplace. We do so through our flexible workplace policy which includes a minimum of 3 days a week onsite. This policy provides the benefits of connecting and collaborating in-person in support of our Mission.

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Reasonable Accommodations

Baxter 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.

Recruitment Fraud Notice

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