Project Coordinator (f/m/d) - R&D Video Integration of Medical Devices at Baxter
München, Bayern, Germany -
Full Time


Start Date

Immediate

Expiry Date

02 Jul, 25

Salary

0.0

Posted On

30 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Ms Project, English, Project Management Skills, Communication Skills, Medical Devices

Industry

Hospital/Health Care

Description

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.

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
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
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