Quality Assurance Associate I - 2nd Shift Employer Siegfried Location Irvine, CA Start date Sep 13, 2026 View more categories View less categories Discipline Quality , Quality Assurance , Quality Control Required Education Bachelors Degree Position Type Full time Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details "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:

The QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release. 2nd

Shift Hours:

2 PM - 10:30 PM Monday through

Friday Your Profile:

Responsibilities QA Production Floor Support Provide Quality support to Manufacturing personnel on the shop floor for compounding and QA- 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, CSIT/PID test, weight check, and torque test. Perform AQL and Level II Visual Inspection for Finished products. 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 comply with cGMP and GDP. Support the issuance of GMP documentation to the Manufacturing floor. QA Batch Review and Product Release Review executed batch records for completeness, accuracy and compliance with approved procedures and Good Documentation Practices (GDP) and resolve discrepancies with manufacturing operators or supervisors. Use computerized systems and software such as SAP, LIMS, and TrackWise for data collection and batch record review. Enter and verify data from executed batch records into the Product Log Sheet and maintain the database up to date at all times. Participate in deviation investigation and CAPA implementation. Initiate Certificate of Conformance and prepare executed batch records for product release in a timely manner to meet compliance requirements and business needs. Scan and file batch records (physically & electronically). Assist in writing and/or revising SOPs to ensure compliance with cGMP and other applicable regulations. Required Knowledge, Skills and Abilities Working knowledge of QA principles In Pharmaceutical and/or other FDA regulated industries required Good computer skills Strong attention to detail Good oral and written communication skills Ability to work overtime and/or work on weekend as needed Required Education and Experience Bachelor's Degree in Biochemistry, Chemistry, Engineering, Biology or closely related discipline required 1-2 years' experience in Quality Assurance / Manufacturing environment in Pharmaceutical or other GMP regulated industries required

Target Pay Range:

$30-32/hour +10% Differential when working on 2nd Shift (2 PM -10:30 PM) Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.

Your Benefits:

Medical, Dental, Vision, Life Voluntary Accident, Hospital, Pet 401K Generous Time Off Structure including PTO, Holidays, Sick & Personal Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 highly skilled professionals, we take the innovations of our pharmaceutical customers to industrial scale and manufacture safe drugs for patients worldwide. As a fully integrated CDMO, Siegfried is one of the few organizations today that can carry out the development and manufacturing of APIs and finished dosage forms under one roof. This unique combination of know-how and experience makes us the most trusted partner in the pharmaceutical industry. Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Engineer Thousand Oaks, California Sr. Engineer, Process Development Thousand Oaks, California Pharmaceutical Finishing Operator Charlottesville, VA