Sr. Technical Document Specialist
On-site · Clayton, North Carolina, United States
Job Summary
Lead and execute labeling component development for Grifols Therapeutic products, coordinating with external typesetters and internal partners to create/revise labeling components, review vendor proofs, and ensure adherence to labeling timelines. Manage labeling documentation and history, review component completeness and accuracy, and coordinate large labeling projects while guiding peers through training or coaching as needed. Requires strong communication with internal customers and external vendors, proficiency with Word/Excel/Open Site Master/WebCenter, and the ability to supervise or guide others. Lead projects, ensure regulatory and quality considerations are integrated, and maintain alignment across supply chain, manufacturing, and engineering for label development.
Required Qualifications
- BS/BA degree in a relevant field and 6 years of related experience. An equivalent combination of education and experience may be considered.
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