2nd Shift QA Associate: Batch Release & Compliance

Siegfried; Irvine (CA); On-site; USD 41,328 - 44,083; Full time

Benefits offered by this job

Medical, Dental, Vision, Life

Voluntary Accident, Hospital, Pet

401K

Generous PTO/Holidays/Sick & Personal

Job summary

Siegfried in Irvine, CA is seeking a QA Associate I for 2nd shift to support QA on the production floor and product release, ensuring GMP compliance and accurate documentation. Responsibilities include line clearance, visual inspection, in‑process sampling, deviation investigations, and batch record review using SAP, LIMS, and TrackWise.

A related bachelor's degree and 1–2 years in QA/manufacturing are required.

Qualifications

• Must have working knowledge of QA in pharma/GMP environments.
• Strong attention to detail and excellent communication skills.
• Willingness to work overtime and weekends as needed.

Responsibilities

• Provide QA support to manufacturing on the shop floor for compounding and in‑process checks.
• Perform line clearance verification, validation tasks and in‑process QA checks.
• Review batch records for compliance and support GMP documentation.

Skills

QA principles

Computer skills

Attention to detail

Oral and written communication

Overtime/weekend availability

Education

Bachelor's degree in Biochemistry, Chemistry, Engineering, Biology or related

Tools

SAP

LIMS

TrackWise

Job description

Siegfried in Irvine, CA is seeking a QA Associate I for 2nd shift to support QA on the production floor and product release, ensuring GMP compliance and accurate documentation. Responsibilities include line clearance, visual inspection, in‑process sampling, deviation investigations, and batch record review using SAP, LIMS, and TrackWise.

A related bachelor's degree and 1–2 years in QA/manufacturing are required.