Our client is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional’s, and branded generic medicines. Our 103,000 colleagues serve people in more than 160 countries.
This position works out of our Temecula, California location in our AVD Vascular business unit. Our solutions are used in hospitals, laboratories, and clinics around the globe. The crucial information derived from our tests, instruments and informatics systems are often the first step in patient care decision making for hundreds of health conditions from heart attacks to blood disorders to infectious diseases and cancers. Our products are also utilized by laboratory management to ensure efficiency in their operations.
Our client provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.
Job Summary: The scope of work will be primarily focused on the AV TEM JI remediation initiative. The engineer will review, and update AV TEM training guides (includes Job Instructions + Job Breakdown sheets) for products produced in the Temecula facility.
Responsibilities:
- Review & 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) - This job will require the engineer to work with line support ME, line supervisors, Operators to ensure there is alignment on changes/corrections to the documents - This job will require the engineer to go into the production lines to review and verify the manufacturing sequences is aligned with the MPI. - This job will require the engineer to train trainers on the changes/updates to the documents - other tasks as assigned
Requirements:
- Min experience 3-5 years with BS degree - Experience using MS office applications - Experience in manufacturing - Experience in creation and/or modification of manufacturing related document instructions - English proficient Plus - Familiar with CO/CR process - Familiar with redlining documents - Familiar with Abbott systems (LHR, viewpoint, sumtotal, blueprint, others) - Training of production personnel - Worked in a clean room environment - Worked in medical devices - Must be motivated, self starter, organized, and can multitask. - Must have good communication skills (verbal and written) - 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) - Manufacturing line support and project management experience - Lean manufacturing is a plus.
Shift: 14:30 pm- 11 pm Hourly range: $30-40/hour
This job description will be reviewed periodically and is subject to change by management.