Quality Engineer - Sterilization
Full Time
Ontario, CA 91710
Posted
Job description
Roles & Responsibilities:
- Is business with Sterigenics, they have a chamber they use for their product. They want to increase the capacity, purchasing a bigger chamber from 3 to 6 pallets. They need to finalize the implementation. Supplier quality is already completed, and validation documentation is already created—they need someone to pick up the work where the other consultant left off.
- Getting a second supplier, with up to 6 pallets. Validation. Steris in Temecula. Also needs QE support for this implementation.
- This person needs to finish the completion of the validations and have a strong sterilization understanding. (ETO)
- There are also ongoing suppliers that they are looking Statistical Data, maybe Chemical Engineering Background
- Run it by the end user, hands on in the packaging area, how we are prepping the product to go out.
- Local Process that needs to be updated. Current chamber is 3 pallets, configuration needs to be changed. Preparation before it goes to Sterilization. Procedural Documentation work is the key
- Validation
- Sterilization Experience, ETO/EO
- Medical Device QE
- Chemical Engineering background
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