Why Join Bracco Medical Technologies?

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way.  Each member of the Bracco Medical Technologies team has the power to make a difference......every day!

The Supervisor, Production is responsible for overseeing the assembly and production of the company’s highly regulated medical devices. This role ensures that all production activities are completed efficiently, on schedule, within budget, and in compliance with quality and customer requirements.

The Supervisor ensures adherence to Good Manufacturing Practices (GMP) and established Quality Systems through effective process management, documentation control, and metric-driven performance oversight. Regular communication and updates to team members are essential to maintain alignment, support daily operations, and ensure successful execution of production plans.

Primary Duties & Responsibilities:

Supervision and Employee Development

• Supervise the daily activities of Assemblers and employees in the assembly of Medical Devices.
• Recruit, select and retain a high-performance Production team
• Balance the assembly lines and test area in relation to availability of staff and demands of daily production schedule
• Set and communicate performance expectations and hold team members accountable for achieving expectations and completing assignments
• Promote and manage employee development and foster employee growth of employees within the production group through:
  • Full-cycle Performance management
  • Skills development
  • Ongoing performance feedback and timely performance appraisal
  • Recognition and motivational techniques/tools to drive high levels of employee satisfaction.

• Manage conflict by dealing effectively with others in an antagonistic situation; use appropriate interpersonal styles and methods to reduce tension and conflict between two or more people

• Oversee and/or conduct training of new or existing employees and facilitates the assimilation of new members and changes.

Production Planning and Inventory

• Execute and offer input to the weekly, quarterly, and yearly production planning activities to maintain output to required inventory levels and customer demand.
• Monitor usage of materials to ensure efficiency of operations. Communicate with planning and procurement on priorities. Perform timely transactions online utilizing ERP/MRP system including Production Orders and the creation of NCMR’s

Quality and Continuous Improvement

• Work closely with the manufacturing engineering and sustaining engineering groups to lead updates and improvements to manufacturing processes. Help develop, update, and maintain procedures and documentation to assure compliance to Quality System and Regulations.
• Maintain process records and metrics data gathering and reporting. Monitor quality of production output products by reviewing routers and test records.
• Initiate and execute change orders and updates to work instructions to ensure continuance of production.

• Develop and recommend improvements to facilities, equipment, or procedures that improve safety, quality, and efficiency.
• Implement existing production and business processes; make adjustments and recommendations as necessary to produce products within specifications.

Audit and Compliance Responsibility

• Work within the company’s quality policy, established business practices and SOP’s (Standard Operating Procedures) to ensure the operations environment is organized, compliant, and maintained.
• Accompany auditors as required.

• Recommend and implement action plans to correct deviations noted during audits.