QA Technician II - 3rdShift

Siegfried•Irvine, CA

1d•$30 - $33

About The Position

Expect to grow", personally and professionally: At Siegfried, we offer exciting challenges and ample opportunities to showcase your talents. As a trusted and respected partner to the pharmaceutical industry, we uphold the highest standards in safety, quality and sustainability, while fostering a culture that empowers you to thrive. Join a rapidly expanding global company, where diverse perspectives and experiences come together in a collaborative environment. Here, you'll find a workplace that values both collective success and your individual contributions—offering long-term opportunities to grow and make an impact. Your Role: This 3rd Shift position supports the Quality Assurance Operation, which consists of QA Production Floor supports, and QA Product Release. 3rd Shift: 10:00 PM - 6:30 AM Sunday Night thru Friday Morning Your Profile: This position supports the Quality Assurance Operation, which consists of QA Production Floor supports, and QA Product Release.

Requirements

Good computer skills
Strong attention to detail
Good oral and written communication skills
Ability to work overtime and/or work occasionally on weekend as needed
General high school degree/GED or equivalent required.
Basic reading, writing, and math skills required.
1-2 years' experience working in a Pharmaceutical, Medical Device, or other FDA regulated industries required.

Nice To Haves

Some college or technical college preferred.
Prior experience working in QA function preferred.

Responsibilities

Provide Quality support to Manufacturing personnel for compounding and in-process checks.
Perform line clearance verification, sterilization chart review, scale calibration verification, and QA in-process checks including but not limited to visual inspection, CISIT/PID test, weight check, and torque test.
Prepare in-process samples for submission to the Quality Control Laboratory.
Support handling of GMP events and initiation of deviation investigations.
Read, understand, and follow SOP’s and complies with cGMP.
Support the issuance of GMP documentation to Manufacturing floor.
Review executed batch records for completeness, accuracy and compliance with Good Documentation Practices.
Use computerized system such as SAP, LIMS, and TrackWise for data collection and batch record review.
Scan and file batch records (physically & electronically).
Perform other work-related duties as assigned by management.