Perform final assemble mechanical device, use adhesive and UV light to bond the parts accordingly the specification of a drawing diagram. Using Borescope inspection for particles, perform line clearance, inputs data in ELHR, insert wires into hyper-tube, measuring the tension and crimp the hyper tube, testing the device according to MPI.

__Inspect incoming materials, and tools. Follow MS to qualify tools and equipment.__Contact supplier for materials discrepancy, managing WIP materials and warehouse materials.__Read and interpret engineering drawing, follow specs to qualify tools and fixture.__Recognize and report any unacceptable materials and/or sub-assemblies to engineer or supervisor.__Shipping, receiving, cycle count, update inventory spread sheet,__Assemble product as required utilizing small hand tools, calibrated instrument, measurement equipment, microscope, solder iron, welding and test fixture.

__Conducting inspection final and incoming parts base on MS for measurement dimensional and functional test.__Perform First Article inspections to qualify tolling. Verify parts with CFC and RoHS certificate compliance.__Create and record detailed observation of none conformances in the Device History Records.__Communicate discrepancy to Quality Engineering, and Supplier Engineering.Input data, record transaction, verify parts and move materials in SAP and ACCS (Agile) system to retrieve, submit on-line documentation.

• Perform assemble medical device, using digital caliper and ruler to verify the tolerance accordingly the specification and drawing diagram.• Receive, unpack, and warehouse in-coming materials and supplies. Check incoming goods against documentation. Sort and count materials and supplies as needed. Perform receipt transactions against open purchase orders in Quickbooks for inventory and non-production materials.• Label incoming materials according to Company procedures. Distribute all materials received to the requisitioner, IQC or to stock. Fulfill production requests for raw materials/floor stock/supplies as needed. Inform Purchasing when raw materials/floor stock/supplies needs replenishment.• Work closely with QC group to manage the logistics of material moved between QC and the warehouse. Work with Customer Service to reconcile any issues relating to sales orders, allocations, ship-to addresses, method of shipment, etc. Cycle count production materials and finished goods as required.

• Perform class III mechanical sub-assembly device called Luna, pull out the parts listed in LHR, verify part number, lot number match the description, and follow the SOP to build sub-assembly, bonding sub-assembly parts. Clean parts in sonic bath; put it in oven for drying. Train new staffs.• Perform inspection, testing the device; verify the functional of the device to ensure the measure the within the tolerance accordingly the specification and drawing diagram. If the functional test fails then proceed the rework process with supervision approval or coordinate with engineer.• Perform line clearance, precede packaging follow the SOP place device in the right box, and insert instruction.

• Follow SOP to build mechanical sub-assembly components, clean parts with IPA, perform microscope to assemble a small sub-assembly part, using a vacuum pen to pick up small piece of thin filter and stacking them in six layers inside a small tube using tweezers to align the filter then precede bonding and curing sub-assembly. • Use software to test digital PCB, test monitor, down load firmware according to SOP.Inspect, test, rework and verifies final subassembly is complete and correct.

• Follow GMP to perform line clearance after the product in the clean room, set up hood for inspection.• Perform visual inspect the solution in vial for contamination and other defect. • Perform MES transaction to move the product out from the warehouse to clean room, perform bulk packaging.• Involved with engineer in Kaizen event to improve manufacturing process. Help modify SOP and monitor equipment for calibration update. Plan daily task schedule, training new staffs, review logbook.

• Follow the SOP to cleaning mandrel in sonic bath with IPA and still water, installed silicon tube, used caliper to measure gauge within specification, loaded stent, set up crimping equipment to crimp stent, used microscope to inspect the stent, set up the hydrophilic machine.• Verified measurement of catheter and leak testing, checking for coating mask.

• Follow SOP to perform manual filling reagent with pipette.• Perform packaging kit reagent; manual label vials, boxes, bags; auto label vials and printing labels; use SAP to transfer product to warehouse. Set up pump for filtration, made buffers, clean glassware, auto clave, setup Flexicon auto-fill. Perform acid and base to adjust the ph. Level and conductivity level. Perform calibrating pipette, balance.• Perform calculating metric math conversion, measurements in volume and concentration.

• Follow SOP to assembled and disassembled granulation, miller, screener, blender, mixer to cleaning and sterilization.• Perform troubleshoot electrical mechanical equipment necessary to manufacture products. • Worked with engineer to set up equipment and raw materials for research new products.• Set up mechanical equipment, monitor equipment’s for calibrating and maintenance