Job Responsibilities:
- Execute production builds both on live WO and under protocols as needed.
- Interpret engineering drawings schematic diagrams or formulas and confer with management or engineering staff to determine quality and reliability standards.
- Read worker logs product processing sheets and specification sheets to verify that records adhere to quality assurance specifications.
- Aid in planning work assignments in accordance with worker performance machine capacity production schedules and anticipated delays.
- Prepare charts graphs and diagrams to illustrate workflow routing floor layouts material handling and machine utilization.
- Observe worker using equipment to verify that equipment is being operated and maintained according to quality assurance standards.
- Observe workers operating equipment or performing tasks to determine time involved and fatigue rate using timing devices.
- Evaluate data and write reports to validate or indicate deviations from existing standards.
Software Skills:
- Ignite PLM (Team center)
- Previous experience with computer applications and software such as MS Project and Excel.
Skills:
- Previous experience working on valves or other cardiovascular medical devices
- Driven product execution and finalizing builds for market release (and lead these efforts)
- Skilled in report documentation authoring and release
- Strong communication skills both verbally and written is REQUIRED this role will have a lot of touchpoints with onsite labs and other facilities driving production
- Lead change requests build coordination and documentation of class II or III medical devices
Education/Experience:
- Bachelors degree in engineering required.
- 57 years experience required.
Education: Bachelors Degree
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