Responsible for shift-to-shift communication to ensure all customer requirements and departmental goals are met.
Lead all departmental meetings.
Work on continuous improvement and “zero defect” operations.
Create and improve departmental documentation.
Train personnel on all new or updated processes and procedures, including ECO’s, press packets, ISO/QS/TS, SPI’s, and customer specifications.
Coordinate with planning personnel to ensure all internal and external customer requirements are met.
Monitor and control operation hours, labor hours, finished goods inventory levels and operating supplies.
Make recommendations to address positive and/or negative standard variances.
Participate as a member of the New Program Development, Quoting, and APQP Teams.
Participate in ISO/QS/TS and Customer internal and external audits.
Promote cleanliness and safety policies and procedures.
Stay current on new technology.
Requirements
BS degree in an Engineering or Plastics related discipline.
Minimum 5 years experience with medical device molding operations.
Experience with ISO 9000, ISO TS 16949 Automotive, ISO 13485 Medical and other customer specific requirements.
Experience with Manufacturing Engineering, Tooling, Engineering, Design and Manufacturing, PFMEA’s, Process Flow Charts, Inspection Control Plans, and statistics.
