Document Control Admin
On-site · Manchester, New Hampshire, United States
Job Summary
Document Control Admin role supporting document control processes and related quality systems in a medical device manufacturing setting. Interfaces with manufacturing, engineering, and project teams to manage change control administration, part number management, BOM structure, and revision control within PLM/ERP systems; review changes for accuracy and impact; facilitate change review and closure; organize and archive controlled documents; ensure QMS documents are reviewed and properly formatted; provide Good Documentation Practices guidance; maintain design history files, device master records, and device history records; proactively communicate requirements and resolve documentation requests with internal and external customers.
Required Qualifications
- Bachelor’s degree or comparable experience
- Experience working in a manufacturing company
- Familiarity with GDP preferred
- Familiarity with ISO 9000 and/or ISO 13485 preferred
- Systems oriented with PLM and/or ERP experience
- Organized, detail oriented, and self-directed; able to meet goals and deadlines without supervision
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