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QC Associate II - 3rd Shift

Job in Irvine, Orange County, California, 92713, USA
Listing for: Siegfried
Full Time position
Listed on 2026-06-26
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 30 - 32 USD Hourly USD 30.00 32.00 HOUR
Job Description & How to Apply Below

"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

QC Associate II, 3rd Shift (10 PM - 6:30 AM Sunday night - Friday morning)

The Quality Control Associate II will execute critical functions to support the manufacturing of sterile drug products. The role supports the Raw Materials team by aseptically sampling incoming goods for chemical and microbiological testing, performs environmental monitoring and evaluates results in an aseptic manufacturing facility, and conducts physical testing using instrumentation and dimensional analysis of components. The Associate will also learn Chemistry and Microbiology analyses to support timely release of In‑Process Control test results and batch release.

Responsibilities
  • Perform sampling of raw materials for chemistry and microbiology testing in clean‑room classified areas, minimizing contamination using aseptic technique.
  • Execute Environmental Monitoring program, including viable and non‑viable sampling and data analysis.
  • Perform sampling and inspection in compliance with cGMP. All activities are performed in a GMP/GDP environment.
  • Support media fills through personnel monitoring, scribing aseptic behavior and reading cultures after incubation.
  • Document raw data contemporaneously and report results promptly. Utilize assigned NB’s and LIMS system.
  • Execute support functions (i.e. washing glassware, preparing media, running autoclave, changing charts).
  • Maintain the working areas in a clean and organized state. Assist in quality oversight of warehouse operations.
Required Knowledge,

Skills and Abilities
  • Able to gown aseptically and maintain certification to internal requirements.
  • Ability to sample aseptically, perform fine measurements using tools and learn new instrumentation.
  • Competency with routine software programs (i.e. MS Word, MS Excel).
  • Aptitude for learning new programs (i.e. Labware LIMS, SAP).
  • Capable of using good reason and judgment to make and defend recommendations.
  • Positive team player in a fast‑paced environment.
Required

Education and Experience
  • B.A or B.S. in Microbiology (preferred), Chemistry or other pharmaceutical‑relevant degree considered.
  • 3+ years of experience in QC or QA (preferred).
  • 3+ years of experience in FDA‑regulated industry (preferred).
Compensation

Target Pay Range: $30–32/hour + 15% shift differential for working on 3rd Shift (10:00 PM – 6:30 AM Sunday night – Friday morning).

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
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Position Requirements
10+ Years work experience
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