Job Description

GENERAL OBJECTIVE:

This role will work closely with the Quality Director, Quality Manager, and Direct reports to ensure the correct and complete Quality Transition Plan and functionality of Medline RCI Hudson. Responsible for maintaining the company's quality system and supporting compliance with FDA, ISO, and Canadian Regulations, and ensuring compliance with quality objectives. Work with management levels at the site to establish goals to achieve a strategic business plan.

RESPONSABILITIES / FUNCTIONS:

•    Ensure compliance with previously determined quality objectives.
•    Maintains Continuous Improvement through quality projects in the assigned area.
•    Manages and optimizes the necessary resources for the assigned area.
•    Reports the weekly and monthly results in the work area to the multidisciplinary group.
•    Reviews and improves manufacturing and inspection procedures based on improvement.
•    Control and improve the training process for inspectors, leaders, and supervisors.
•    Establishes development metrics in the positions of supervisors, leaders, and inspectors.
•    Verify and update Documents in ETQ. Reliance.
•    Establishes the acceptability of the processes and confirms the correct inspection process in the manufacturing lines.
•    Authorizes substitutions and deviations generated during the assembly process.
•    Attends room/area results control meetings with the multidisciplinary group.
•    Conducts investigations of customer complaints directly related to manufacturing.
•    Produces Quality Cup and Line Bonus reports according to the established policies.
•    Generate and Implement Improvement Ideas
•    Participate on MKO’s Implementation strategies

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, disability/handicap status or any other legally protected characteristic.