Quality/Document Control Intern

Quality & Document Control Summer Intern Company: ANEUVO Job Type: Internship — Summer 2026 Duration: 10–12 Weeks Compensation: Paid About ANEUVO Aneuvo develops neuromodulation technologies and software platforms that improve patient outcomes and empower clinicians with advanced diagnostic and therapeutic tools. We work at the intersection of hardware, firmware, software, data, and biomedical innovation. Our Product Support Engineers ensure customers and internal teams can rely on our neuromodulation systems with confidence. Position Overview The Quality & Document Control Summer Intern will support ANEUVO's Quality Assurance and Document Control teams in maintaining integrity, accuracy, and compliance of critical business and operational documentation. This is an excellent opportunity for a detail-oriented student to gain real-world exposure to quality management systems (QMS), regulatory standards, and controlled document processes within a professional environment. Key Responsibilities Assist in the creation, review, revision, and maintenance of controlled documents including SOPs, work instructions, forms, and policies Support document lifecycle management — including version control, document routing, and archiving — within the company's QMS or DMS platform Conduct document audits to verify accuracy, completeness, and compliance with internal and regulatory standards Assist with tracking and closing corrective and preventive actions (CAPAs) and non-conformance reports (NCRs) Participate in internal quality audits and gap assessments Support the preparation of reports and quality metrics dashboards Collaborate cross-functionally with engineering, operations, and compliance teams to ensure documentation aligns with current processes Identify opportunities for process improvement and document workflow optimization Qualifications Required: Currently enrolled in an accredited college or university program in Quality Engineering, Industrial Engineering, Business Administration, Life Sciences, or a related field Strong attention to detail and commitment to accuracy Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) Excellent written and verbal communication skills Ability to manage multiple tasks and meet deadlines in a fast-paced environment Preferred: Familiarity with quality management standards such as ISO 9001, ISO 13485, FDA 21 CFR, or GMP/GxP Experience with document management systems (e.g., Veeva, MasterControl, Documentum, SharePoint) Prior coursework or experience in quality assurance, regulatory affairs, or compliance Basic understanding of CAPA, root cause analysis, or audit processes What You'll Gain Hands-on experience with a functioning Quality Management System Exposure to industry-standard document control practices and regulatory frameworks Mentorship from experienced quality and compliance professionals A meaningful project with measurable outcomes to add to your portfolio Networking opportunities within a growing, innovative organization #J-18808-Ljbffr