Quality Documentation Intern
Cretex Medical
About the Role
Quality Documentation Intern - Summer 2027
Location: Bloomington, MN
Key Responsibilities
- Scan quality records, and verify scan quality, page counts and completeness.
- Help 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.
- Understand customer needs and the core business markets we serve.
- Maintains an organized work area.
- Partners with other business segments as needed.
- Work with Device History Records (DHR) and Device Master Records (DMR) when needed.
- Completes all other work duties as assigned.
Requirements & Tech Stack
- Enrolled in a two-year technical program or a four-year degree program.
- Demonstrated software application skills in Word, PowerPoint, and Excel.
- English language (reading and writing).
- Experience with general office equipment, such as a copier, printer, fax machine and scanner.
- Strong verbal and written communication skills.
- Excellent interpersonal and team building skills to create effective working relationships with suppliers, and coworkers.
- Ability to prioritize work and manage multiple tasks when needed.
- Ability to focus and maintain accuracy while doing highly repetitive work.
- Good attention to detail.
Pay Range
USD $23.00 - USD $23.00 /Hr.