Jobbeschreibung
Step out of your comfort zone, excel and redefine the limits of what is possible. That's just what our employees are doing every single day – in order to set the pace through our innovations and enable outstanding achievements. After all, behind every successful company are many great fascinating people.
In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. All of this is supported by a special ownership structure and the long-term goal of the Carl Zeiss Foundation: to bring science and society into the future together.
Join us today. Inspire people tomorrow.
Diversity is a part of ZEISS. We look forward to receiving your application regardless of gender, nationality, ethnic and social origin, religion, philosophy of life, disability, age, sexual orientation or identity.
Apply now! It takes less than 10 minutes.
-
take care of the correct collection, preparation and upload of our UDI database to e.g. U.S., South Korea or EU
-
assessing future UDI requirements and implementing identified requirements into our existing Quality Management System
-
provide and support work package(s) within the currently running UDI Project
-
take responsibility for Life cycle concerning UDI / label activities like establishing a print validation, correct UDI integration within the product change process, time management, data upload and preparation of documentations and rollouts
-
operate stakeholder management with internal and external partners for our collaboration on SAP Add ons (currently U.S. and EU)
-
maintaining the test plan for SAP Add in collaboration with Corporate IT and Master Data Management, correct possible bugs and ensure a correct upload process proactively
-
supporting creation/maintaining of relevant standard operating procedures and work instructions,
-
take care of the specifications, technical drawings and reports for different labels
-
a master's degree in medical technology / engineering or equivalent
-
knowledge of UDI requirements according to (EU) 2017/745 MDR and advantageously experience with further country UDI requirements
-
existing empirical values with UDI database(s) including upload and data maintenance
-
project management skills including application of relevant tools and methods
-
experience in the design and optimization of processes
-
beneficially professional experience in medical technology (including but not limited to UDI and label requirements) and quality management (ISO 13485, MDSAP)
-
professional competence in the use of MS Office products
-
a structured, independent and implementation-oriented way of working with good teamwork and communication skills
-
high level of motivation, additionally to the willingness to take on responsibility and familiarizing with new topics
-
very good English writing and speaking skills, German as a plus