Quality Systems Document Control

Role: Temporary Document Control Support specializing in the management and review of quality and regulatory documents within a biopharma setting. Objectives: ensure document compliance, facilitate review/approval workflows, and support QMS software implementation. Responsibilities: interact with global stakeholders, create/revise/release documents, maintain document lifecycle, and support special projects. Qualifications: HS diploma or higher (preferably Bachelors in English or technical writing), experience in administrative, quality, or document control roles, proficiency in MS Office, SharePoint, Adobe Acrobat, and strong attention to detail. Skills: effective written/verbal communication, organizational ability, and understanding of formal QMS document management. High-Value: role involves GxP compliance, document control within quality systems, and support for biopharma regulatory standards. Work setup: hybrid (minimum 3 days onsite), temporary (6-8 months), with physical requirements related to office work. No specific therapeutic areas or development stages specified, but focus on supporting document workflows for quality assurance and regulatory compliance.