Packaging Supervisor - 2nd Shift- Ave Maria, FL.

Arthrex, Inc.•Ave Maria, FL

50d•Onsite

About The Position

Arthrex Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex Manufacturing is actively searching for a Packaging Supervisor to work at our Ave Maria, FL. Location on the Second Shift. The successful candidate will manage finished device production through the effective use of resources while adhering to the Arthrex Quality Management System and company policies and procedures. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better. Second Shift - 4:00pm - 2:30am, Monday- Thursday, Tuesday- Friday, (rotating Schedule)

Requirements

High school diploma or GED equivalent required
Bachelor's degree preferred or an Associate's degree with related experience. Non-degreed candidates with direct experience in an FDA regulated industry will be considered
5 years of experience in manufacturing or distribution required OR 3 years of progressive manufacturing experience AND a bachelor's degree.
3 years of leadership experience preferred.
Leadership and decision making skills needed
Strong communication, problem-solving and conflict resolution skills
Ability to learn new systems quickly to perform most job functions
Presentation skills required
Intermediate Microsoft Office Skills:
Able to navigate through SAP without guidance in order to perform job functions and possesses ability to assist personnel as needed
Critical Thinking - Using logic and reasoning to identify the strengths and weaknesses of alternative solutions, conclusions or approaches to problems
Excellent verbal, written, analytical, project, research, organizational and interpersonal skills with a sharp attention to detail and the ability to handle multiple priorities simultaneously
Ability to read and understand Bills of Material (BOMs), Routers, drawings and Work Instructions in written or graphical form
Ability to work independently and interact with all levels of management
Ability to define problems, collect data, establish facts, and draw valid conclusions
Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables
Ability to comprehend and apply mathematical principles to the degree required to perform the job based upon job requirements.
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

Experience in medical devices or another highly regulated industry is preferred
Experience in a Lean manufacturing environment preferred
Experience with SAP preferred

Responsibilities

Accountable for managing, meeting, and reporting Key Performance Indicators on Packaging operations.
Resolve work order and inventory discrepancies.
Review master production schedule and make recommendations for schedule changes that optimize resources.
Coordinate activities with other functional groups such as Component Manufacturing, Supply Chain, Quality, Engineering, Validation and Sterilization to ensure on-time delivery.
Liaison with Engineering and Quality Assurance in relation to non-conformances, process deviations, assembly design issues, and continuous improvement initiatives.
Hire, discipline and discharge employees with the assistance of HR.
Ensure compliance by all employees to policies and procedures.
Monitor personnel training & ensure documentation of required training activities is completed.
Perform periodic performance feedback, formal performance reviews and handle disciplinary actions.
Monitor attendance and perform time clock management.
Assign personnel and direct workflow
Assist employees with professional development/training
Communicate issues to management that could result in process delays, safety issues, or other potential loss to the company or its associates
Ensure proper communication between shifts and crews covering production status, backorders, quality, safety and other production issues
Monitor and execute corrective actions to reduce/eliminate scrap
Perform Safety training for direct reports
Maintain inventory accuracy for assigned area
Stay current with ISO/FDA and internal quality assurance policies