| Location | Crystal Lake, IL |
| Job Type | Full-time |
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 Specialist II's overall purpose is to work as a member of the Quality team to support the overall health and compliance of the Quality Management System in alignment with ISO 13485 regulations. This role will have a heavy focus on the maintenance of the quality management system (QMS), with direct support and/or ownership of the document and record control, change management, and training processes. The Quality Specialist II will be responsible for supporting the administration and maintenance of electronic systems implemented for the management and maintenance of the QMS. The Quality Specialist II works under general supervision of the Quality Director.
Requirements
Shift available:
**NO PHONE CALLS PLEASE!! We will contact applicants for an interview if interested. Thank you.