This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
The UDI and Data Management specialist will manage and take tactical, and operational decision, related to our UDI system, related QMS documentation, training and other product data management tasks.
Job Responsibility
Manage UDI and other data management related projects and activities
Ensure that all of the activities to assure compliance to UDI regulations are fulfilled with regards to publishing data to authorities
Secure solid communication within Mölnlycke for product master data including overview of interface to other systems using data (PIM, RR etc)
Give guidance to our global organisation with regards to UDI and other master data submissions (e.g EHS, Sustainability data)
Initiate and monitor CRUD-matrix for product master data
Securing business requirements to enable failsafe data transfer integrations between PLM, ERP-systems and integrated systems
Organizing and participating in stakeholder and governance meetings for UDI
Applicable dialogue with UDI suppliers
Develop and host necessary trainings for UDI and master data related topics
Responsible for taking stakeholders perspective into considerations
Develop required QMS-documentation within UDI
Data management information on the Hub - Introduction to newcomer, e.g., explanation of data management and system landscape
Tactical and operational decision on global UDI roadmap
Decisions focusing on improving processes and practices with regards to UDI and product data management
Requirements
Minimum 5 years in relevant business area
Minimum bachelor's degree in engineering or Life Sciences or equivalent business experience
Experience from working in PLM, UDI, ERP-systems and managing product master data
Knowledge with design control related to medical devices (e.g ISO 13485/ CFR part 820) is an advantage
Understanding of GDSN, authority databases (e.g GUDID, EUDAMED) and relevant healthcare/medical device industry is an advantage
Nice to have
Knowledge with design control related to medical devices (e.g ISO 13485/ CFR part 820) is an advantage
Understanding of GDSN, authority databases (e.g GUDID, EUDAMED) and relevant healthcare/medical device industry is an advantage