IV Fluids Quality Engineer (Must Have Life Science, Pharma Environment)

Title: IV Fluids Quality Engineer (Must Have Life Science Pharma Environment)

Location: San Diego CA

Contract Term: 6 Months

Shift/Hours: 1st Shift ( 8-9am to 4-5pm) / 40hrs

Client: Medical Device Company

Job Category: Engineering

Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)

No H1Bs

Quality Engineering is responsible for review and release of documentation for the release of IV Fluids solutions. Engineer must have experience with the Life Science Pharma industry having device manufacturing experience a big plus.

The IV Fluids Quality Engineer is responsible for:
Supporting the release of IV Fluid Solution product documentation
Creation updating and maintenance of quality documentation required to release IV Solutions
In this role you will be responsible for quality assurance of the warehouse and logistics processes
You will support the business in implementing the legal regulatory and other requirements in the area distribution for regulated products (drugs medical devices)
Reviews and approves change control documentation and specifications (e.g. initial process introduction complaints) is also part of your area of responsibility
You are responsible for supporting corporate audits
Another important part of this role is participating in the release (review) of new IV Fluid solutions specifications.
Supports and approves IV Fluid Solutions documentation in accordance with requirements
Supports the operations quality team as required

Requirements:
BS in technical field (Engineering Life Science)
5 Years experience in a life science Pharma environment
Experience with medical devices a gig plus
SAP knowledge
MS Office Suite