Components Technician I

We Are Blood•Austin, TX

6d•Onsite

About The Position

As a Components Technician, you manufacture blood components using high tech equipment, in an assembly line environment. We Keep Austin Weird in a regulated lab, safely, and in compliance with departmental operating procedures, AABB and FDA Guidelines and cGMP. As needed, back up Hospital Services by assisting with blood drive pick ups. Meet and exceed customer expectations and adhere to established quality practices while seeking to continually improve work performance. Shift: TBD

Requirements

High school diploma or equivalent.
Familiarity with personal computers and/or blood processing systems.
Must be at least 21 years of age with a valid Texas driver’s license, an acceptable driving record and proof of insurance.
Ability to stand for extended periods.
Ability to lift 30 pounds.
Demonstrated ability to be detail oriented.
Manual dexterity and good hand/eye coordination.
On call scheduling requires flexibility.
Documented experience that demonstrates fine motor skill coordination. Demonstrate ability to multi-task in a fast paced regulated environment.

Nice To Haves

Experience in a regulated environment is preferred.

Responsibilities

Manufacture plasma for transfusion, plasma for further manufacturing, cryoprecipitate, pooled cryoprecipitate, whole blood derived platelets and red blood cell products in compliance with department SOP, cGMP and package inserts. Create all components appropriately in the We Are Blood computer
Inspect and determine visual acceptability for all blood products throughout manufacturing steps.
As assigned, perform QC activities in accordance with Standard Operating Procedures that include but are not limited to reviewing daily temperature monitoring documents, documenting centrifuge quality control. Verifying technical services scales are within target values and performing product quality control
Complete all documentation accurately with strict adherence to cGMP and SOP.
Be responsible for monitoring all product storage equipment and take appropriate action in the occurrence of out-of-temperature events.
Report all product deviations to the Components Manager, TS Management, or QA, in a timely and professional manner.
As needed, complete blood center documentation (SIR, Equipment Problem Reports) completely and in a timely and thorough manner, in accordance with SOP and cGMP.
Prepare recovered plasma shipments as well as shipment documentation in accordance with SOP, cGMP and fractionators’ requirements.
Own the experience by meeting and exceeding customer service standards for internal and external customers.
Meet and exceed employee program expectations of AMO CommYOUnity! standards: Rewards & Recognition, Communication, Individuality, Integrity, Respect, and Pursuit of Excellence.
Special projects as assigned.