Battelle delivers when others can’t. We conduct research and development, manage national laboratories, design and manufacture products and deliver critical services for our clients—whether they are a multi-national corporation, a small start-up or a government agency. We recognize and appreciate the value and contributions of individuals from a wide range of backgrounds and experiences and welcome all qualified individuals to apply. Job Summary The Project Quality Specialist provides project support to medical device product development teams. This role prepares documentation packages for data collection, completes document reviews in alignment with Good Documentation Practices (GDP), manages post‑processing and routing (including DocuSign/e‑signature envelopes), performs document review and reconciliation, and serves as a backup witness for testing activities. The Specialist partners closely with project members across multiple disciplines – engineering, quality, project managers, customers – to maintain complete, accurate records under an ISO 13485 compliant Quality Management System.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
Number of Employees
5,001-10,000 employees