WI3814584

1

Vocational Degree

Associate Degree

Unspecified

40

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