Technipaq is family owned and operated serving the medical device and pharmaceutical packaging industry since 1984. We started as a small one machine company and now operate over 160,000 square feet of manufacturing space with 3 manufacturing and warehouse facilities and 180+ employees. Our manufacturing facilities perform the laminating, slitting, sheeting, die cutting, fabricating, and flexographic printing of pouches, lids and roll stock produced in a variety of sizes from foil, film, Tyvek and paper laminates. We offer employees a full benefits package including medical, dental, vision, paid Sick and Vacation time, 401(k) with a company match, and paid holidays.
The Quality Engineer's overall purpose is to work within the Quality team to ensure the quality of the company's products are in line with ISO 13485 compliance. They are responsible for understanding the underlying quality issues, developing successful fixes, and changing practices where necessary to ensure that standards are maintained. The Quality Engineer works with the Engineering, Production, and Management teams, Technipaq suppliers and customers and plays a key role in fixing issues when they arise. The Quality Engineer works under minimal supervision of the Quality Director.
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Required Skills:
The Quality Engineer's overall purpose is to work within the Quality team to ensure the quality of the company's products are in line with ISO 13485 compliance. They are responsible for understanding the underlying quality issues, developing successful fixes, and changing practices where necessary to ensure that standards are maintained. The Quality Engineer works with the Engineering, Production, and Management teams, Technipaq suppliers and customers and plays a key role in fixing issues when they arise. The Quality Engineer works under minimal supervision of the Quality Manager.
**NO PHONE CALLS PLEASE!! We will contact applicants for an interview if interested. Thank you.
| Location | Crystal Lake, IL |
| Job Type | Full-time |
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