Medical Device Development Technician II/III

Cretex Companies, Inc.

Dassel (MN)

On-site

USD 34,632 - 56,026

Full time

14 days+

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Job summary

Cretex Medical is seeking a Development Engineering Technician to support high-volume medical device manufacturing. You will assemble prototypes, execute tests, document results, and help improve processes.

The role includes maintaining tooling, fixtures, and setup of equipment while collaborating with engineers and manufacturing teams. Qualified candidates bring minimum 3 years as an engineering technician (Level II/III), CAD know-how (AutoCAD/SolidWorks/Pro-E), and strong communication,

Qualifications

3 years of experience working as an engineering technician (Engineering Technician Level II/III).
Prior chemical handling experience strongly preferred.
Knowledge of Good Manufacturing Practices & Quality Systems Regulations is desirable.
Medical product experience.
Must have good communication and documentation skills.
Must have problem solving and critical thinking skills.
Working knowledge of CAD software platforms AutoCAD, SolidWorks, or Pro-E experience is desired.
Ability to cross train in other areas of production when required.
Microsoft Office proficiency (Outlook, Word, Excel, PowerPoint, Publisher).
Clear and effective verbal and written communication skills.
Attention to detail.
Organizational skills.
Ability to work in a fast-paced team environment.
Ability to prioritize and multitask.

Responsibilities

First point of contact for technical support escalation for operations.
Provide assembly process feedback to the engineering team.
Conduct tests, measures and collect data in support of validation activities.
Responsible to monitor, inspect, setup, calibrate, and maintain manufacturing process equipment.
Research and identify manufacturing or engineering solutions.
Diagnose and troubleshoot technical issues, including but not limited to, machining, injection molding, laser processing, stamping, or packaging.
Assist engineers as they create, modify, and test products and processes.
Inspect products and processes for flaws and identify areas of improvement.
Reads and complies with work instructions, set up sheets, and checklists.
Enters production information/data into the ERP/Quality system on a timely basis.
Generate ECO/DCO and process documentation changes related to manufacturing changes, such as work instruction changes, print changes, documentation updates, etc.
Perform equipment set-ups as required.
Support and comply with the company Quality System, ISO, and medical device requirements.
Read, understand, and follow work instructions and standard work.
Partner with other business segments: sales/marketing, customer service, engineering, quality, and finance.