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Join a global leader in life science and diagnostics as a Project Document Specialist supporting product lifecycle documentation and document control activities. In this role, you’ll ensure technical documents, drawings, and project records are complete, accurately categorized, and compliant with data integrity standards while supporting document workflows within Veeva QualityDocs.
Job Responsibility
Review, process, and maintain product lifecycle documentation through Veeva QualityDocs
Ensure documents, drawings, and technical data are complete, accurate, and compliant with document control procedures
Support document approval workflows while maintaining data integrity standards
Identify documentation gaps, proofread records, and communicate issues or questions promptly
Collaborate with cross-functional teams to obtain clarifications and resolve documentation discrepancies
Manage multiple document requests and priorities in a fast-paced environment
Perform detailed, repetitive document review tasks with a high degree of accuracy and consistency
Requirements
Associate's degree or higher in a technical discipline
1–2 years of direct document control experience
Experience working with enterprise Document Management Systems (eDMS)
Veeva QualityDocs experience is highly preferred
Proficiency with Microsoft Office Suite and SharePoint
Strong attention to detail with excellent proofreading and organizational skills
Self-motivated, dependable, and comfortable working independently in a remote environment
Excellent communication skills with the ability to collaborate across multiple departments