Senior Pharma Labeling Graphic Designer (Regulatory)

Sanofi

Cambridge (MA)

On-site

USD 85,000 - 110,000

Full time

14 days+
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Job summary

Sanofi is seeking a Senior Graphic Designer to create and manage pharmaceutical product labeling artwork for the U.S. and Canada, ensuring compliance with regulatory standards.

The role involves detailed layouts, graphic development, and timely delivery across multiple sites. The candidate will leverage Adobe Illustrator and MAC-based workflows, collaborating across cross-functional teams to maintain high-quality deliverables and accurate regulatory text while supporting continuous process

Qualifications

  • Bachelor’s degree in graphic design or related field.
  • 3+ years of pharma packaging artwork experience in regulated environment.
  • Strong knowledge of FDA labeling regulations, GMP standards, and MAC-based production systems.

Responsibilities

  • Develop and implement creative solutions for continuous process improvement.
  • Support Artwork Transformation.
  • Manage files and computer systems.
  • Read and interpret packaging component specification drawings.
  • Comply with GMP regulations.
  • Maintain electronic artwork library for components and prescribing information.
  • Provide technical support for MAC systems and graphic arts design issues.
  • Prepare artwork for multiple sites (domestic/international).

Skills

Graphic design
Adobe Suite
Regulatory compliance
GMP knowledge
Detail oriented
Communication
Project management

Education

Bachelor's degree in Graphic Design

Tools

Illustrator
MAC systems

Job description

Sanofi is seeking a Senior Graphic Designer to create and manage pharmaceutical product labeling artwork for the U.S. and Canada, ensuring compliance with regulatory standards.

The role involves detailed layouts, graphic development, and timely delivery across multiple sites. The candidate will leverage Adobe Illustrator and MAC-based workflows, collaborating across cross-functional teams to maintain high-quality deliverables and accurate regulatory text while supporting continuous process

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