Job Description

Job Description:

• Review documents for accuracy, clarity, and consistency of content and format; correct spelling, grammar, and punctuation.
• Electronic proofreading software experience, a plus.
• Highlight (for additional review) other non-grammatical inconsistencies observed such as with artwork or layout when proofreading materials.
• Coordinate and collaborate with internal stakeholders to ensure delivery timelines are met.
• Composition copy, SPL, core template; coordinate with other Coordinators and Labeling Specialists to meet delivery standards and deadlines.
• Verify language sources from SmPC and USPI for international markets; mark up inconsistencies and escalate to Labeling Specialist for review and remediation.
• Ensure recent major USPI changes are applied, verifying hyperlinks in annotated documents and ensure accuracy of cross references in labeling.

Required:

• minimum of 1 year of labeling proofreading experience in a regulated environment, or at least 3 years other specialized proofreading or pharmaceutical experience.
• Prior experience proofreading, preferably in a regulated environment, including use of a range of tools.
• Demonstrated capabilities in meticulous work practices, attention to detail and working in a team environment.
• Proficiency in standard office technology, including the Microsoft Office Suite.
• Good understanding of pharmaceutical or medical terminology.

Ideal Candidates Would Also Have:

• Familiarity with labeling-related regulations and industry practice a plus.
• Experience in proofreading, including prescription drug labeling.
• Prior experience with electronic proofreading tools a plus.