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Packaging Supervisor - 2nd Shift- Ave Maria, FL

Job in Ave Maria, Collier County, Florida, USA
Listing for: Arthrex
Full Time position
Listed on 2026-01-01
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Production Manager
Job Description & How to Apply Below
Position: Packaging Supervisor - 2nd Shift- Ave Maria, FL.
Location: Ave Maria

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

Requisition  |

Title:

Packaging Supervisor - 2nd Shift
- Ave Maria, FL. | Division:
Arthrex Manufacturing Inc (US02) |

Location:

Ave Maria, FL.

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).

Essential Duties and 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.
Education / Experience
  • 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.
  • Experience in medical devices or another highly regulated industry is preferred.
  • Experience in a Lean manufacturing environment preferred.
  • Experience with SAP preferred.
Skills
  • 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.
Specific Duties and Responsibilities
  • 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.
Knowledge

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.

Reasoning Ability

Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical…

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