Med Device Document Control Specialist

MedSource Labs LLC; Chanhassen (MN); On-site; USD 45,000 - 60,000; Full time

Job summary

MedSource Labs LLC in Chanhassen, Minnesota is looking for a Document Control Specialist to enhance quality management processes. The specialist will ensure accurate document filing and adherence to regulatory standards while collaborating with various departments. Applicants should possess a high school diploma with 1-3 years of relevant experience, and familiarity with the medical device industry is preferred. The role includes data management, document approvals, and process improvements in a collaborative environment.

Qualifications

• 1-3 years' experience preferred in a relevant field.
• Understanding of FDA and ISO regulatory requirements.
• Prior experience in document control within medical device or pharmaceutical industry is desirable.

Responsibilities

• Ensure compliance with regulatory and internal policies.
• Manage data entry, data management, and report generation.
• Transition paper files into the eQMS.
• Oversee review and approval of controlled documents.
• Coordinate document retrieval requests from internal stakeholders.

Skills

Attention to detail

Written and verbal communication

Document management systems

Process improvement

Education

High School Diploma or Equivalent Experience

Tools

Excel

Microsoft Outlook

PowerPoint

Job description

MedSource Labs LLC in Chanhassen, Minnesota is looking for a Document Control Specialist to enhance quality management processes. The specialist will ensure accurate document filing and adherence to regulatory standards while collaborating with various departments. Applicants should possess a high school diploma with 1-3 years of relevant experience, and familiarity with the medical device industry is preferred. The role includes data management, document approvals, and process improvements in a collaborative environment.