Ra Professional Artwork Management Emea - 1-year Contract

Johnson & Johnson Johnson & Johnson · Pharma · Warsaw, Masovian, Poland

This role is for an RA Professional focused on Artwork Management within the EMEA region for Johnson & Johnson's Innovative Medicine division. The primary responsibilities include using artwork management systems, coordinating artwork approval, entering data for tracking, and liaising with various internal and external stakeholders to ensure timely implementation of packaging materials while minimizing costs. The role requires previous experience in Regulatory Affairs and artwork management, proficiency in English, and accuracy with deadlines.

What you'd actually do

  1. Use of Artwork management System to initiate artwork for new labelling or changes to current labelling into production and/or generation of mock-up needed for regulatory submissions
  2. Complete review of the artwork (using electronic tool, where possible) and co-ordinate the final approval of the artwork with Local Operating Companies driven by the agreed deadlines.
  3. Entering data and using tools to monitor metrics for tracking of implementation of packaging material
  4. Liaise with Local Operating Companies Regulatory Affairs, quality, Product Artwork, supply chain, packaging sites internal/external to meet both Health Authorities implementation timelines and minimize current stock /component write off costs
  5. Performing and/or co-ordination of Quality Check (QC) of local Product Information
  6. Communication with local stakeholders of the Local Operating Companies in scope during the review process

Skills

Required

  • Previous experience of 2 years in Regulatory Affairs and artwork management
  • Proficient level of English
  • Accuracy, precision and respect of timelines is mandatory

Nice to have

  • Experience of working in a virtual team and/or global organization
  • Experience in working with limited supervision and able to make independent decisions
  • Knowledge of multiple languages

What the JD emphasized

  • Accuracy, precision and respect of timelines is mandatory