Global Regulatory Labeling Specialist (Medical Devices, W2)

Redbock - an NES Fircroft company; Irvine (CA); On-site; USD 80,000 - 120,000; Full time

Job summary

A leading medical device firm located in California is seeking a Regulatory Affairs Specialist to manage global labeling compliance. The role involves owning labeling deliverables for product development, ensuring compliance with various global standards, and managing change control activities. Ideal candidates will have 5–9 years of relevant experience and a Master's degree in a related field. This opportunity promises to be a significant contribution to innovative medical device projects.

Qualifications

• 5–9 years of labeling and compliance experience.
• Experience in medical device regulatory environments.

Responsibilities

• Own regulatory labeling deliverables for new product development.
• Ensure compliance with EU MDR and global labeling standards.
• Manage labeling change control activities.

Skills

Detail-oriented

Collaborative

Regulatory compliance

Labeling standards

Education

MS in Science, Engineering, or Regulatory

Job description

A leading medical device firm located in California is seeking a Regulatory Affairs Specialist to manage global labeling compliance. The role involves owning labeling deliverables for product development, ensuring compliance with various global standards, and managing change control activities. Ideal candidates will have 5–9 years of relevant experience and a Master's degree in a related field. This opportunity promises to be a significant contribution to innovative medical device projects.