Manager Supplier Quality Management (m/w/d) at Baxter
Lowa, Tasmania, Germany -
Full Time


Start Date

Immediate

Expiry Date

19 Nov, 26

Salary

0.0

Posted On

21 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Manufacturing

Description

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

For our Saalfeld (Thuringia) location, we are looking for a Manager Supplier Quality Management (m/f/d) .

Your tasks

  • They are responsible for supplier quality management.
  • They ensure the conformity testing of the products, including incoming goods inspection.
  • If necessary, initiate corrective actions with suppliers.
  • They are responsible for supplier audit management.
  • They operate in an international environment and work with local as well as global suppliers.
  • They take over the management of employees.

Your profile

  • Education: at least 4 years of completed university education in a technical or medical technology field (ideally with a focus on quality management)
  • Professional experience: Several years of professional experience in quality management (>5 years)
  • Fluent English and German skills
  • Experience working with diverse cultures and employees
  • Practical knowledge of regulatory requirements and quality system requirements for medical devices (EN ISO 13485, EU MDR)
  • Experience in audit management
  • Experience with SAP
  • Confident demeanor, assertiveness, and independent work style


Responsibilities
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