Quality Documentation Coordinator (2)

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