UDI Data Support (Medical Devices)- Essity
Skill Kompetenspartner AB / Biomedicinjobb / Mölndal
2026-05-29
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hela Sverige About the company
Essity Mölndal is part of the global hygiene and health company Essity, present in 150 countries. It is a global leader within hygiene and health products, operating in an international and highly regulated environment where quality, compliance, and innovation are central parts of the business. You will become part of a global organization working closely with cross-functional teams across business, IT, regulatory affairs, and master data functions.
About the role
We are now looking for an experienced consultant within UDI Data Support to support ongoing and future UDI (Unique Device Identification) activities within a global medical device organization.
In this role, you will collaborate closely with the Global UDI Data Business Manager and support the organization in anticipating and managing global UDI regulatory requirements. The role involves cross-functional collaboration with stakeholders across business, IT, regulatory affairs, R&D, packaging development, master data, and commercial teams.
You will play an important role in ensuring data readiness, governance, compliance, and alignment between regulatory requirements and operational processes.
The role includes responsibilities such as:
UDI & Regulatory Support
• Interpret and translate global UDI regulatory requirements into business and data specifications * Support the development of plans related to UDI data preparation and submissions * Coordinate implementation progress, stakeholder alignment, and issue resolution across functions * Support work related to data readiness, governance, and consistency in line with current and future UDI data models * Support the creation of UDI-related processes and documentation within the quality management system (QMS) * Support and potentially educate internal stakeholders and departments regarding UDI-related processes and requirements
Cross-functional collaboration & systems
• Work closely with stakeholders across Regulatory Affairs, R&D, IT, Packaging Development, Master Data, and Commercial teams * Contribute to data-driven processes and system-related initiatives connected to UDI activities * Support reporting, presentations, and documentation related to ongoing projects and regulatory requirements * Participate in process improvements and help ensure effective collaboration across functions and geographies
Your profile
We are looking for someone who has experience working in global and cross-functional organizations, preferably within the medical device industry or other highly regulated environments.
You are comfortable interpreting complex requirements and translating them into structured and practical actions connected to processes, systems, or data management.
To succeed in this role, we see that you have:
• Experience working with regulatory, technical, or data-driven processes * Strong communication and stakeholder management skills * Experience working in cross-functional and international environments * Ability to work in a structured and organized way with strong attention to detail * Experience creating documentation, reports, presentations, or QMS-related material * Good understanding of business processes and system support
We also see it as meritorious if you have: * Experience within Medical Devices, Regulatory Affairs, or R&D * Experience working with UDI frameworks or UDI implementation * Experience related to master data or governance processes * Experience collaborating with IT teams on system-related initiatives * Experience with SAP S/4HANA
Personal qualities
As a person, you are collaborative, structured, and solution-oriented. You enjoy working across functions and building strong relationships with stakeholders in different parts of the organization.
You are proactive, communicative, and comfortable working in environments where priorities may change and where not all processes are fully defined from the beginning.
Additional information
The assignment is hybrid, with a preference for being on-site approximately two days per week. For the right profile, a fully remote setup can also be considered.
The preferred start date is as soon as possible, ideally around July 1st. The assignment scope is flexible between 80-100% depending on availability. The selection is ongoing, so please submit your application as soon as possible.
Interviews are planned for the end of week 24 and, if needed, the beginning of week 25. If you have any questions, you're very welcome to contact the responsible recruiter, Maria Haswani, at
maria.haswani@skill.se Så ansöker du Sista dag att ansöka är 2026-06-05
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "teamtailor-7821910-2026054".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Skill Kompetenspartner AB (org.nr 556685-8618),
https://jobb.skill.se Första Långgatan 18 (
visa karta)
413 28 GÖTEBORG
Jobbnummer 9937180