Pharma MAP Proofreader – Detail-Driven Content Auditor

Zenith LifeScience LLC.; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

Zenith LifeScience LLC. is seeking a meticulous Proofreader for US Commercial Operations. The role focuses on ensuring MAP materials and promotional content strictly reflect approved content with high quality across platforms and events.

Responsibilities include validating copy, communicating risks to stakeholders, and supporting content integrity to meet marketing launch timelines. Pharma experience is preferred but not required, with emphasis on attention to detail.

Qualifications

• Minimum 3 to 4 years proofreading experience.
• Exceptional attention to detail and meticulousness.
• Strong proofreading skills are essential.
• Solid understanding of the English language.
• Proven ability to manage multiple priorities under tight deadlines.
• Proven ability to deliver high-quality work in a fast-paced environment.
• Experience with Veeva PromoMats software.
• Preferred: TVT software knowledge.

Responsibilities

• Content accuracy gatekeeper: Rigorously proofread and validate all documents to ensure they precisely match approved content in a variety of platforms and environments.
• Consistent and urgent communication: Proactively communicate key findings and potential risks to stakeholders and verify discrepancies with impacted stakeholders.
• Support content integrity: Review and validate copy against Source of Truth documents, ensuring every word is correct and consistent.
• Assist with other related tasks as needed to support our US marketing operations team and goals.

Skills

Proofreading

Attention to detail

Multi-tasking

English proficiency

Communication

Team player

Evening/weekend availability

Tools

Veeva PromoMats

TVT

DocuProof

Microsoft Word

Microsoft Excel

Job description

Zenith LifeScience LLC. is seeking a meticulous Proofreader for US Commercial Operations. The role focuses on ensuring MAP materials and promotional content strictly reflect approved content with high quality across platforms and events.

Responsibilities include validating copy, communicating risks to stakeholders, and supporting content integrity to meet marketing launch timelines. Pharma experience is preferred but not required, with emphasis on attention to detail.