Project Coordinator (f/m/d) - R&D Video Integration of Medical Devices

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.

Baxter Medical Systems enables excellence in surgical procedures in modern medical technology. From emergency care to critical care, our products help care teams achieve outstanding results. To enable surgical staff and multidisciplinary care teams to work efficiently, digital systems are automated and devices are essential to streamline processes, increase user convenience and improve patient safety. Baxter takes this development into account and sets new standards with its intelligent and networked solutions.

We are currently searching a Project Coordinator (f/m/d) for our Sustaining Team in R&D Video Integration of Medical Devices based in Munich.

Responsibilities:

• Planning and controlling of change projects
• Monitoring of project execution including project reporting
• Design controls to ensure development quality
• Creation, optimization and maintenance of product-related documentation
• Working closely with quality and product management, regulatory department and service department to ensure customer satisfaction
• Coordination of external development partners
• Coordination of complaint investigations

Education & Work Experience:

• University degree in a relevant engineering discipline or equivalent
• Several years of professional experience in product development
• Experience in a medically regulated environment (EN ISO 13485, euMDR, 21 CFR 820, Medical Design Controls, risk management for medical devices) desirable
• Project management skills
• Project planning skills (e.g. MS Project)
• Strong organizational and communication skills
• Independent, structured, autonomous and solution-oriented working style
• Enthusiasm and motivation
• Business fluent in English and good written and spoken German

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.

Have we sparked your interest?

If you like the sound of the above role, can thrive in a fast-paced working environment and are passionate about working in a learning and growth culture, then we’d love to talk to you. Apply direct on our  Online System.

For further information, please reach out to Teresa Feilhuber via E-Mail: teresa_feilhuber@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.

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