- Review and update AV TEM training guides (includes Job Instructions + Job Breakdown sheets) for products produced in the Temecula facility
- Review and assess the content of the training guides to ensure it lines up with the manufacturing instructions (MPI)
- Correct for any gap/fixes (i.e. redline/update documents, initiate COs)
- Work cross-functionally with line support in ME, line supervisors, and operators to ensure there is alignment on changes/corrections to the documents
- Go into the production lines to review and verify the manufacturing sequences is aligned with the MPI
- Train trainers on the changes/updates to the documents
- Experience using MS office applications
- BS in Engineering
- Entry level position with 1 -3 years of experience in a manufacturing environment
- Experience in manufacturing (hands-on)
- Experience in creation and/or modification of manufacturing related document instructions
- English proficient
- Familiar with CO/CR process
- Familiar with redlining documents
- Familiar with LHR, viewpoint, sumtotal, blueprint, others a plus
- Training of production personnel
- Worked in a clean room environment
- Worked in medical devices
- Must be motivated, self starter, organized, and can multitask
- There is no traveling, but will require some flexibility on hours (to be aligned with production schedule and line support ME hours)
- Will require to stand for extended periods of time (while in the clean room)
- On-site in Temecula, CA
- First round of interviews will be by phone or video call, second round will be in-person.
- 6-month contract starting 6/17/24-EOY
- Pay rate: Starting at $30/hr
- Business Unit: Vascular
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Manufacturing Engineer - Temecula, United States - GForce Life Sciences
Description
Manufacturing Engineer 1 – Temecula, CA
Must be able to work on a W2
Duties
Qualifications
Term & Start