Quality Assurance Specialist II

Technipaq

  • Crystal Lake, IL
  • 5 days ago
  • Full-time

Highlights

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. 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.

Numbers & Facts

LocationCrystal Lake, IL
Job TypeFull-time

Description

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

  • 2 - 4 years previous administrative support within a QA capacity in an ISO certified manufacturing environment required.
  • Associate or bachelor's degree preferred.
  • Must be at least 18 years of age and pass our pre-employment Reading and Ruler tests.
  • Previous experience leading and participating in customer and supplier audits in an ISO 13485 environment preferred
  • Proficient in MS Office including Word and Excel required.
  • Previous experience performing internal audits preferred
  • Working knowledge of calibration systems and/or ISO Internal Audit experience preferred.
  • Strong organizational skills and the ability to effectively communicate and share knowledge with others is also required.

Shift available:

  • 8:00 am to 4:30 pm M-F

**NO PHONE CALLS PLEASE!! We will contact applicants for an interview if interested. Thank you.

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