Supervisor - Milling and Drill Cell

Arthrex•Ave Maria, FL

9d•Onsite

About The Position

Arthrex Manufacturing in Ave Maria, FL is looking to find someone to lead a high-performing team across Milling, Drill Cell, and EDM in this Supervisor – Component Manufacturing role, where this individual will drive operational excellence and ensure alignment with production goals. In addition, will also oversee, manage, and provide direction to the manufacturing department that will effectively and profitably meet or exceed internal and/or external client expectations by delivering superior quality products and service. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

Requirements

High school diploma or GED equivalent required
5 years of manufacturing experience required, preferably in a machining environment OR 3 years of progressive manufacturing experience AND a bachelor’s degree.
3 years of leadership experience required within a machining environment, five or more preferred.
Proficiency with standard MS Office desktop applications (Word, Excel, Outlook) is required
Demonstrated process improvement skills
The ability to prioritize, work in a fast-paced environment, handle multiple tasks, and work under time constraints
Able to communicate effectively, in both written and verbal formats, using spoken and written English
Must have leadership skills and be able to effectively supervise and motivate team members
Ability to interpret a variety of instructions furnished in written, oral, diagram, and / or schedule form
Lathes preferably Swiss, Milling Machines and Wire EDM’s
Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures.

Nice To Haves

Bachelor’s degree is preferred.
Experience in a Lean manufacturing environment is desirable
Experience in medical devices or another highly regulated industry is preferred

Responsibilities

Recommends proper staffing levels based on production needs for area of responsibility
Monitors production plan by consistently meeting daily production schedules and reports status
Gives input for introduction of new products and processes into the plant
Ensures operator rotation program is functional
Recognizes and addresses process problems regularly
Assures proper maintenance of equipment and tooling
Monitors employee performance through goal setting
Perform attendance and time clock management
Ensures proper communication between shifts and crews covering production status, backorders, quality, safety and other production issues. Including communication to managers and fellow supervisors.
Ensures daily housekeeping and organization standards are followed
Reviews, counsels, evaluates, disciplines, hires and discharges employees with the assistance of HR
Comply with LEAN initiatives and create culture of accountability in a LEAN environment
Provides employees with development/training opportunities.
executes corrective actions to reduce/eliminate scrap
Performs Safety training for direct reports. Monitor areas for potential hazards.
Ensures compliance by all employees to policies and procedures
Stays current with ISO/FDA and internal quality assurance policies