QA Technician Assistant II - 1st Shift

BioSpace; Irvine (CA); On-site; USD 37,000 - 44,000; Full time

Benefits offered by this job

Medical, Dental, Vision, Life

Voluntary Accident, Hospital, Pet

401K

Generous Time Off Structure including

PTO, Holidays, Sick & Personal

Job summary

Siegfried is seeking a Quality Assurance Technician to join our team in Irvine. You will work with Manufacturing and Quality squads to ensure products are manufactured safely, in compliance with FDA and GMP, and meet the highest quality standards.

As a QA Technician, you’ll perform in-process inspections, review documentation, and help drive deviations investigations while using SAP, LIMS, and TrackWise to maintain regulatory compliance and product integrity.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Quality Assurance

Documentation

Attention to detail

Communication skills

Education

High School Diploma or GED

Tools

SAP

LIMS

TrackWise

Job description

"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

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.