Operator I

Responsible for the production of high-quality medical devices within a manufacturing cell. Under close supervision, performs assembly, repair, and testing of pacemakers, implantable cardioverter defibrillators (ICDs), leads, and related medical device components while following standardized procedures and quality standards.

• Perform assembly, repair, and testing operations on medical devices and components.
• Follow standardized procedures and work instructions.
• Ensure all products meet quality and regulatory standards.
• Maintain accurate production and quality documentation.
• Ensure full traceability of parts and components.
• Support Quality Management Systems (QMS), Environmental Management Systems (EMS), and regulatory requirements.
• Participate in continuous improvement and Lean Manufacturing initiatives.
• Identify and communicate production issues and improvement opportunities.
• Maintain accurate traveler and quality records.
• Communicate clearly (written and verbal) with supervisors and management.
• Maintain a positive attitude with internal teams and external visitors (tours).
• Collaborate with supervisors to set and monitor performance goals and metrics.
• Support divisional initiatives as required.

• High school diploma or equivalent.
• Ability to read, understand, and follow written and verbal instructions.
• Basic understanding of Lean Manufacturing principles.
• Ability to use electronic data collection systems and computer software.
• Strong attention to detail and documentation accuracy.
• Ability to prioritize tasks effectively.
• Ability to handle and maneuver small components.
• Ability to make decisions with minimal supervision.
• Work is closely supervised and continually reviewed.
• Must follow strict safety guidelines.
• Ability to work with small parts and in a controlled production environment.