Global Labeling Proofreader: Precision & Compliance

Cardinal Health; United States; On-site; USD 37,000 - 48,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Paid time off plan

Health savings account (HSA)

401k savings plan

Access to wages before pay day with my

Flexible spending accounts (FSAs)

Short- and long-term disability

Work-Life resources

Paid parental leave

Healthy lifestyle programs

Job summary

Cardinal Health is seeking a Proofreader - Global Labeling to ensure 100% accuracy, consistency, and regulatory compliance of global labeling and packaging graphics for medical devices. You will read, analyze, and compare ts against proofs to detect errors and provide feedback to designers.

The role requires attention to detail, collaboration with labeling engineers and regulatory affairs, and adherence to GDP and international regulatory standards.

Qualifications

• Bachelor's degree in English, Technical Writing, Life Sciences or related field.
• 2+ years of professional proofreading in a regulated environment preferred.
• Experience with labeling, packaging or regulatory documents is highly desirable.

Responsibilities

• Proofreads labeling and regulatory graphics for grammatical, typographic and localization accuracy.
• Verifies artwork packages and ensures alignment with source documents and translations.
• Collaborates with labeling engineers, regulatory affairs and design teams to implement changes.

Skills

Attention to detail

Communication skills

Ability to provide actionable feedback

Education

Bachelor's degree in English or related field

Tools

Adobe Acrobat

Microsoft Office

PDF comparison software

PLM software (Windchill, Agile, SAP)

Job description

Cardinal Health is seeking a Proofreader - Global Labeling to ensure 100% accuracy, consistency, and regulatory compliance of global labeling and packaging graphics for medical devices. You will read, analyze, and compare ts against proofs to detect errors and provide feedback to designers.

The role requires attention to detail, collaboration with labeling engineers and regulatory affairs, and adherence to GDP and international regulatory standards.