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Regulatory Labeling & UDI Specialist

Original title: Regulatory Labeling & UDI Specialist (m/w/d)

Akkodis · Mannheim, Baden-Württemberg, Germany · Remote · Senior

  • Mannheim, Baden-Württemberg, Germany · Remote
  • German

Indexed (today) · refreshed constantly

Start
flexible
Work mode
Remote
Contract
Freelance / B2B
Seniority
Senior
Reference
JN-112026-84066

Required skills

Languages: German

Job description

The company is seeking a Regulatory Labeling & UDI Specialist for a full-time, contract role in the medical technology sector. The position involves managing product labeling, UDI data, and regulatory documentation.

Project overview

We are looking for a Regulatory Labeling & UDI Specialist

  • Creation, review, updating, and versioning of product labels, packaging information, and associated regulatory product information
  • Implementation of regulatory requirements for labeling and product information, especially in the context of EU MDR and IVDR
  • Processing and maintenance of UDI-relevant information, particularly UDI-DI, UDI-PI, and associated master product data
  • Maintenance and management of relevant product and regulatory data in Polarion
  • Coordination of label and artwork changes, including review, approval, and documentation processes
  • Creation, updating, and management of Instructions for Use (IFU) and support for the implementation and maintenance of eIFU
  • Execution and documentation of changes within defined change management processes
  • Coordination with relevant interfaces from Regulatory Affairs, Quality, Product Management, Engineering, and other project-related departments
  • Several years of project experience in the labeling, regulatory, or product information environment of medical technology
  • Sound knowledge of regulatory requirements for Medical Devices or In-vitro Diagnostics, especially EU MDR and/or IVDR
  • Practical experience with UDI, UDI-DI, UDI-PI, and regulatorily relevant master product data
  • Experience in the creation, review, approval, and versioning of labels, artwork, and packaging information
  • Experience with IFU/eIFU and the management of digital instructions for use
  • Knowledge of Polarion or comparable systems for requirements, documentation, or product data management
  • Experience with structured change, review, and approval processes in a regulated environment
  • Independent, structured way of working and experience in collaborating with different departments
  • Start: short notice / by arrangement
  • Duration: 3-6 months +, with option for extension
  • Workload: Full-time
  • Location: Remote / by arrangement
  • Industry: Medical Technology / Medical Devices

Project details

  • Start: flexible
  • Location: Mannheim, Baden-Württemberg, DE
  • Languages: German

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