Document Control & Training Specialist

The Document Control & Training Sr. Specialist will manage Document Control activities and perform training-related tasks to support the Training Program. The individual will advance and implement document management processes and perform document administration tasks in Veeva QualityDocs, ensuring that documents are in compliance with GxPs and Good Documentation Practices.

Requirements

• Bachelor’s degree or higher
• Minimum 5 years of experience in a quality assurance role in the pharmaceutical industry required
• Experience with EDMS and LMS systems, preferably Veeva Quality Docs and Veeva Training
• Excellent knowledge and understanding of applicable GxP regulations
• Experience in the identification and resolution of Good Documentation Practices issues
• Familiarity with Microsoft Office Suite, Docusign, Smartsheets, Sharepoint, Adobe Pro, etc.
• Ability to work in a fast-paced environment with excellent multitasking skills
• Must have attention to detail
• Works with minimal supervision
• Must have effective technical writing skills
• Requires excellent organizational, interpersonal, and communication skills
• Must exhibit professional behavior and be aware of the importance of teamwork within the assigned department

Benefits

• $110,000 - $125,000 a year