Job Description

• processing, tracking and archive of GxP documentation both hardcopy and electronic documentation.
• managing (log, QC, process, track, scan, file, label, index, etc.) as required physical and electronic documentation and perform quality checks in accordance with procedures to ensure that GxP documentation is accurate and complete.
• Supporting training management including but not limited to administrative tasks related to on-boarding, creating quizzes, formatting SOPs and other documents, etc.
• Will support regulatory inspection preparation and onsite during inspections as required.
• This position will be a hybrid role including both remote and onsite days
• Other projects may be assigned as required by business needs

• B.S. Degree in Life Sciences, Chemistry, Engineering or equivalent
• 1+ Years of Document Control Experience in a regulated industry
• Experience with Veeva or similar document control system is preferred but not required.
• Experience processing paper documents preferred but not required
• Comfortable with Microsoft Suite Software including but not limited to word, excel, project, powerpoint, etc.

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