EMEA Regulatory Artwork Manager — 1-Year Contract

Johnson & Johnson Innovative Medicine; Województwo mazowieckie; On-site; PLN 95,000 - 152,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Job summary

Johnson & Johnson Innovative Medicine seeks a Regulatory Affairs Professional Artwork Manager for the EMEA region to be based in Warsaw, Poland or Cairo, Egypt. This is a one-year fixed-term contract opportunity.

You will manage artwork inputs, labeling changes, and quality checks, coordinating approvals with LOCs to meet timelines and maintain data accuracy across global teams. Strong English and cross-cultural collaboration are essential.

Qualifications

• Bachelor's degree with 2+ years in Regulatory Affairs and artwork management.
• Master's degree would be an asset.
• Experience in working with virtual/global teams is an asset.
• Able to work with limited supervision and make independent decisions.
• Cultural sensitivity and ability to thrive in a multi-cultural environment.
• Proficient in MS Office; English proficiency required.

Responsibilities

• Prepare artwork input files or annotated artwork for mockups or creation.
• Use artwork management system to initiate artwork for new labeling or changes for regulatory submissions.
• Perform quality check review of artwork and coordinate final approval with LOCs within timelines.
• Enter data and use tools to monitor metrics for labeling tracking and artwork actions.
• Communicate with internal and external stakeholders across teams to agree on timelines.
• Support standardization/new systems to improve efficiency and business continuity.

Skills

Regulatory Affairs

Artwork Management

MS Office

English Proficiency

Education

Bachelor's degree

Master's degree (asset)

Job description

Johnson & Johnson Innovative Medicine seeks a Regulatory Affairs Professional Artwork Manager for the EMEA region to be based in Warsaw, Poland or Cairo, Egypt. This is a one-year fixed-term contract opportunity.

You will manage artwork inputs, labeling changes, and quality checks, coordinating approvals with LOCs to meet timelines and maintain data accuracy across global teams. Strong English and cross-cultural collaboration are essential.