Experience Inc. Jobs

JOB REQUIREMENTS: Give hope. Give health. Make your mark in the fight against cancer. At Accuray, we make a direct and powerful impact on the lives of cancer patients every day - helping them live longer, better lives. But our commitment to innovation offers a truly unique opportunity: the chance to change the fight against cancer - helping to develop, introduce and support new treatment delivery systems and software that will give new hope and new health to cancer patients and cancer survivors around the world. Accuray develops, manufactures and sells radiotherapy systems for alternative cancer treatments. Our radiation therapy for cancer makestreatment shorter, safer, personalized and more effective, ultimately enabling patients to live longer, better lives. Job Description Summary: We are seeking a motivated and detail-oriented Document Control Intern to support our team with document management tasks, including data entry, report generation, and updates in MasterControl, a leading document management system. This internship is an excellent opportunity to gain hands-on experience in the medical device industry while learning about regulatory compliance and document control practices. Essential Duties and Responsibilities: Data Entry: Accurately enter and update document information in MasterControl, ensuring compliance with regulatory standards. Report Generation: Prepare and distribute routine and ad-hoc reports from MasterControl as requested by various departments. Document Management: Assist in organizing, tracking, and maintaining documentation, ensuring accessibility and version control. Process Support: Support document review, approval workflows, and archival processes as needed. Audit Preparation: Assist in preparing documentation and records for internal and external audits. Compliance: Follow company and regulatory requirements for document management, including FDA, ISO 13485, and other applicable standards. Team Collaboration: Work closely with cross-functional teams, including Quality Assurance, Regulatory Affairs, Research & Development, and Manufacturing, to ensure smooth document workflows. Qualifications: a. Required Currently pursuing an Associate\'s or Bachelor\'s degree in Business Administration, Quality Management, Life Sciences, or a related field. Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint). Experience with MasterControl or similar document management systems is a plus. Strong ability to maintain accuracy in data entry and documentation. Ability to manage multiple tasks and prioritize effectively in a fast-paced environment. Excellent verbal and written communication skills. Willingness to learn new systems and processes in a regulated... For full info follow application link. We are an Equal Opportunity, Affirmative Action employer. Minorities, women, veterans and individuals with disabilities are encouraged to apply. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/9FAA22C8413542E9