Responsibilities:

Coordinating, proofreading, formatting, and troubleshooting issues for controlled documents supporting the manufacturing and testing of products.
Balancing and prioritizing documents to ensure meeting document change request due dates.
Aligning with all levels of the organization to meet the needs of documentation system users on site and at external facilities.
Managing tasks in a fast paced environment while maintaining focus on quality and compliance with SOPs, policies and directives, and regulatory requirements.
Supporting training sessions for system users on making document changes and reviewing electronic reference copies of documents.
Actively demonstrates company values of accountability, quality, efficiency, customer service, collaboration and safety.

Requirements

4-6 years of experience in the pharmaceutical industry, preferably within Quality or Documentation function
Experience with Electronic Documentation Management System is preferred
Proficient in Microsoft Office
Proficient in advanced functions of Microsoft Word
Excellent verbal and written communication