Onsite in Billerica, MA 3 days a week.

Quality Document Associate

Responsibilities:

• Work with stakeholders to manage the transition into eForms from paper and electronic-based forms.
• Create from existing documents eForms in TrackWise Digital
• Project manage multiple data alignment activities as it relates to documentation and training
• Track metrics and generate reports summarizing the findings and providing clear documentation for future reference
• Manages multiple tasks in a fast-paced and dynamic environment while maintaining focus on quality and compliance with local SOPs, policies and directives, and regulatory requirements

Basic Qualifications

• Education/Experience Qualifications: AS in English or Science
• Document Control and/or technical writing experience preferred
• A combination of education, training, and experience may be considered instead of the above-stated qualifications
• Persona example: This position is site-based and requires a presence on-site three days per week

Other Requirements

• Experience in the pharmaceutical industry , preferably within the Quality
• Must have experience in TrackWise Digital
• Must have experience using, creating, and processing eForms in TrackWise Digital
• Proficient in Microsoft Office
• Proficient in advanced functions of Microsoft Word
• Excellent verbal and written communication
• Ability to work independently
• Able to identify and present solutions that will resolve issues and meet the required due dates for documents
• Ability to work in a team environment
• Attention to detail

Some overtime may be required