Sr Ra Professional

Johnson & Johnson Johnson & Johnson · Pharma · Beijing, China

This role is in Regulatory Affairs, focusing on product submissions and registration within Johnson & Johnson's healthcare sector. Responsibilities include reviewing and documenting product inserts, package labels, and artwork, maintaining labeling E2E activity tracking systems, and supporting local labeling initiatives. The role requires collaboration with various cross-functional teams to ensure labeling processes comply with local regulations and global standards.

What you'd actually do

  1. Product Insert, Package Label and Artwork QC review and documentation
  2. Labeling E2E activity tracking system maintenance
  3. Support local labeling initiative
  4. Implement local labelling E2E process to comply with local regulations and globalstandards.
  5. Collaborate with cross functions including XJP CQ, R&D QM, AP, global labelling CoE, andlocal/global cross-functions to ensure labeling process implementation and compliance.

Skills

Nice to have

  • Coaching
  • Communication
  • Competitive Landscape Analysis
  • Compliance Management
  • Design Thinking
  • Detail-Oriented
  • Industry Analysis
  • Market Research
  • Package and Labeling Regulations
  • Problem Solving
  • Product Packaging Design
  • Program Management
  • Quality Assurance (QA)
  • Regulatory Affairs Management
  • Regulatory Compliance
  • Researching
  • Safety-Oriented
  • Sustainability
  • Sustainable Packaging

What the JD emphasized

  • Implement local labelling E2E process to comply with local regulations and globalstandards.
  • Collaborate with cross functions including XJP CQ, R&D QM, AP, global labelling CoE, andlocal/global cross-functions to ensure labeling process implementation and compliance.