Jobs · Management · Michigan

Process Technician I

Medbio, LLC · Grand Rapids, MI · 8 mo ago
ManagementInternship

Major Duties and Responsibilities

  • Provide machine set up and process support for all production processes
  • Review first shots for major defects before quality obtains samples parts
  • Clean, stage and tear down molds (with extreme care and attention) to meet production needs
  • Communicate in an effective and timely manner any equipment issues/breakdowns to maintenance
  • Communicate in an effective and timely manner any automation issues/break to the automation team
  • Communicate in an effective and timely manner any tooling issues to the Production Manager, Process Engineer, and Tool Room Manager
  • Barrel/screw cleaning as needed
  • Troubleshoot minor machine, hot runner, automation, and tooling issues
  • Run sample parts and facilitate in establishing processes for new and transfer tooling projects
  • Work with material handlers in supporting production
  • Exhibit safety awareness and safe work practices

Organizational Relationships

  • The Process Technician I reports directly to the Process Engineer for technical direction and training.
  • The Process Technician I reports to the Team Supervisor for daily work priorities.
  • Team Supervisors and the Production Manager will provide the scheduling priorities for the Process Technician I.
  • Engineering samples or prototype runs will be scheduled in conjunction with the Process Engineer and the Production Manager to avoid complications.

Experience and/or Educational Requirements

  • A High School Diploma or GED equivalent.
  • Prefer two-year certificate or Associates Degree in plastics-related subject.
  • Prefer at least 4 years experience with plastics injection molding set-up and processing duties.
  • Good mechanical aptitude.
  • General understanding of automation systems and equipment.
  • Basic computer skills (Microsoft Office).
  • Basic blueprint reading skills.
  • Strong written/verbal communication, leadership, interpersonal and motivational skills.
  • Understanding of ISO and FDA/GMP regulations with regard to production processes and documentation practices.

Physical Requirements

  • Must be able to work a standard 40 hour workweek with occasional overtime including weekends as a possibility.
  • Sitting and/or standing for an extended period of time as well as some walking within the facility.
  • Must be able to see with or without corrective lenses and distinguish color differences and depth perception for product and safety issues.
  • Hearing ability should be sufficient to hear and react to audible alarms from distances up to 100 feet.
  • The ability to lift and carry various items up to 70 pounds.

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