QA Technician Assistant II - 1st Shift
siegfried · Irvine, CA ·
- Category
- QA
- Experience
- 1+ years
- Company size
- 1000+
- Salary
- USD 27 – 32 / hour
A QA Technician Assistant ensures pharmaceutical manufacturing compliance with FDA/GMP standards by performing in-process inspections, reviewing documentation, and supporting quality systems (SAP, LIMS, TrackWise) during 1st-shift operations (6 AM–2:30 PM).
"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:
Are you detail-oriented, quality-focused, and looking to grow your career in the pharmaceutical industry? Join our Quality Assurance team and play a critical role in ensuring products are manufactured safely, consistently, and in compliance with FDA and GMP regulations.As a Quality Assurance Technician, you'll work directly alongside Manufacturing and Quality teams to monitor production activities, perform in-process inspections, review documentation, and help ensure every batch meets the highest quality standards.
Your Profile:
1st Shift Position: 6 AM - 2:30 PM, Monday - Friday
What You'll Be Doing
- Provide on-the-floor QA support for pharmaceutical manufacturing operations
- Perform line clearances, in-process inspections, and quality checks
- Review batch records and manufacturing documentation for accuracy and compliance
- Prepare samples for Quality Control testing
- Support deviation investigations and GMP event documentation
- Utilize quality systems including SAP, LIMS, and TrackWise
- Help maintain a state of compliance with cGMP and regulatory requirements
What We're Looking For
- 1-2 years of experience in pharmaceuticals, medical devices, or another FDA-regulated industry
- Previous QA experience preferred
- Strong attention to detail and commitment to quality
- Solid computer, documentation, and communication skills
- High School Diploma or GED required; college coursework or technical training preferred
Why Join Us?
- Gain hands-on experience in a pharmaceutical CDMO environment
- Work closely with Manufacturing, QC, and Quality Systems teams
- Build valuable GMP and regulatory compliance expertise
- Contribute directly to the production of products that impact patient health and safety
Target Pay Range: $27 - 32/hour
(1st Shift Hours: 6 AM - 2:30 PM, Monday - Friday)
Individual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.
If you're looking for an opportunity to develop your Quality career in a fast-paced pharmaceutical manufacturing environment, we'd love to hear from you.
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.