Quality Specialist II

New Team LLC•Forest Lake, MN

11d•$26 - $32•Onsite

About The Position

Velosity Forest Lake is seeking a Quality Specialist II to provide support for handling nonconforming material, CAPA requests and reports, and for preparing certificates of conformance and associated order quality related documentation. This is an on-site position supporting our Forest Lake location, with a shift of Monday-Friday 7:30 am - 3:30 pm. Velosity Forest Lake is a state-of-the-art, custom contract manufacturer and injection molder founded in 1972, providing creative solutions to unique manufacturing challenges. Our culture and values, including Collaboration, Results-Driven, Continuous Improvement, Integrity, and Customer Satisfaction, are our competitive advantage.

Requirements

Demonstrated ability to lead initiatives and to complete tasks efficiently and accurately.
Excellent interpersonal and communication skills; effective business correspondence and reporting.
Working knowledge of Microsoft Office and business operating systems.
Knowledge of accepted quality systems; working knowledge of Microsoft Office and IQMS or similar system.
Ability to perform daily tasks safely and to work independently with limited supervision.
Ability to solve practical problems and prioritize multiple tasks to work effectively with customers, vendors and other departments.
Must have correctable eyesight and good depth perception.
Must be a U.S. Citizen, lawful permanent resident (green card holder), or foreign national granted refugee or asylee status.

Nice To Haves

Three-five years of experience in quality with minimum of two years in plastic injection molding or equivalent.

Responsibilities

Work cooperatively with all employees.
Create and review Certification of Conformance (CoC) documentation and associated quality documentation. Maintain and update Product Certification Requirement QMS document.
Initiate MRBs and ensure containment for suspect products.
Coordinate MRB work orders for Rework and Sort Dispositions, including inspection verification and labor entry into Quality System.
Initiate corrective actions and complete effectiveness verifications for product related concerns associated with complaints.
Prepare reports based on Quality System database information for the MRB process. Coordinate periodic reviews based on the reports.
Backup to create and update SPC files.
Coordinate source inspection, as requested.
Make recommendations for continual improvement of documentation systems.
Perform configuration audits and present results to management.
Other tasks as assigned by supervisor.