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Amneal Pharmaceuticals
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Document Level Publishing Specialist

Document Level Publishing Specialist

Amneal Pharmaceuticals

1 - 5 years

|

1 - 6 Lacs

Posted:1 day ago| Platform:

Apply

Skills Required

Regulatory Affairs Documentation Regulatory Documentation

Work Mode

Work from Office

Job Type

Full Time

Job Description

Role & responsibilities

Collaborate closely with the Submission Level Publisher to ensure timely and accurate document processing.
Perform daily PDF processing tasks as per assigned workload and project requirements.
Adhere strictly to submission timelines and regulatory deadlines.
Conduct troubleshooting using ISI Toolbox, resolving technical issues efficiently to avoid delays.
Execute quality control (QC) checks of PDF files, focusing on:

Bookmarking
Hyperlinking
Table of Contents (TOC) accuracy

Implement corrections in processed PDF files based on QC comments or review feedback.
Escalate and communicate any processing issues to the Submission Specialist, particularly those involving ISI Toolbox.
Ensure all files follow Amneal's internal file naming conventions for consistency and traceability.
Actively participate in group activities and provide peer support within the team for eCTD submissions and related publishing tasks.

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