Quality Documentation Coordinator (2)
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Job ref:
9044
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Location:
Billerica, United States
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Sector:
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Contact:
Lissa Jerez
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Published:
almost 2 years ago
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Consultant:
#
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