Quality Documentation Intern - Medical Devices (Summer)

Regulatory Jobs; BLOOMINGTON (MN); On-site; USD 26,000 - 37,000; Full time

Benefits offered by this job

401k match

Onsite health clinics

Discretionary holiday bonus

Cretex University

Job summary

QTS in Bloomington, MN is hiring a Summer Quality Documentation Intern to support the Quality Department with document control projects, scope definition, and implementation.

You will gain exposure to FDA and ISO regulations, document control processes, and cross-functional collaboration within the Cretex Medical family. This internship offers hands-on learning in a fast-paced environment with a focus on accuracy, teamwork, and professional growth.

Qualifications

• Enrolled in a two-year technical program or a four-year degree program.
• Proficient with Word, PowerPoint and Excel.
• Strong English reading and writing skills.

Responsibilities

• Scan quality records and verify scan quality, page counts and completeness.
• Process controlled documents through the QTS documentation system.
• Learn about QTS Quality System requirements and FDA and ISO regulations.
• Learn about document control and documentation control requirements.
• Help retrieve support documentation when needed.

Skills

Word

PowerPoint

Excel

English

Communication

Interpersonal

Teamwork

Prioritization

Attention to detail

Education

Two-year technical program

Four-year degree program

Tools

Document control system

Scanner

Job description

QTS in Bloomington, MN is hiring a Summer Quality Documentation Intern to support the Quality Department with document control projects, scope definition, and implementation.

You will gain exposure to FDA and ISO regulations, document control processes, and cross-functional collaboration within the Cretex Medical family. This internship offers hands-on learning in a fast-paced environment with a focus on accuracy, teamwork, and professional growth.