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QC Chemist III

Job in Irvine, Orange County, California, 92713, USA
Listing for: Siegfried Ltd
Full Time position
Listed on 2026-03-10
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 40 - 48 USD Hourly USD 40.00 48.00 HOUR
Job Description & How to Apply Below
QC Chemist III page is loaded## QC Chemist III locations:
Irvine, CAtime type:
Full time posted on:
Posted 2 Days Agojob requisition :
R26 157"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 Chemist III acts as a senior member of the QC Analytical team supporting raw material and finished product release, stability studies and method qualifications. The Chemist III provides advanced technical expertise in chromatographic analyses (HPLC/GC) and serves as chromatography subject matter expert within the laboratory. As a senior member of the team, this position assists with technical writing (Quality Investigations, Methods, Reports), instrument troubleshooting and laboratory improvement initiatives.
*
* Your Profile:

**##
*** Responsibilities
* ** 1.
Independently execute complex QC chemistry testing to support routine manufacturing activities and stability programs.
2.
Provide advanced technical expertise in HPLC and GC methods including assay, impurities, cleaning validation and stability-indicating methods.
3.
Troubleshoot chromatographic methods and diagnose instrument performance issues. Coordinate minor repairs and vendor service as needed.
4.
Participate in protocol design and execution for method transfers, verificationsverifications, and validations.
5.
Assist in the performance of internal and external audits.
6.
Assume role of SME and trainer for chromatography techniques and instrumentation.
7.
Author or review laboratory investigations (OOS, OOT, Deviations) and technical reports.
8.
Maintain laboratory working areas in a clean and organized state.
9.
Utilize Labware 8 LIMS and chromatography data systems for review and approval activities.
10.
Provide technical support to other departments within the organization.
11.
Any and all other duties assigned by immediate supervisor.##
*** Required Knowledge,

Skills and Abilities

**** Knowledge of quality systems, FDA, ICH and compendial requirements.
* Demonstrated excellence in LC/GC analyses.
* Experience executing method qualifications in a GMP environment.
* Strong troubleshooting and root cause investigation skills.
* Excellent written/oral communication skills.
* Competency with routine software programs (MS Word, MS Excel).Proficient in Microsoft Excel and Word,  Empower, Chromeleon, Track Wise, CDS systems and Lab Ware 8 for data analysis, chromatographic processing, quality management, and laboratory information management.
* Aptitude to utilize advanced laboratory systems (Labware 8 LIMS, CDS systems).
* Capable of using good reason and judgment to make and defend recommendations.
* Positive team player in a fast-paced regulatory environment.##
*** Required

Education and Experience
**** B.S  / M.S Chemistry
* 8+ years of experience in a Chemistry Laboratory
* 5+ years of Experience in a GMP QC Laboratory
* Experience in sterile drug product testing (Preferred)
* 2+ years leadership or mentoring experience (Preferred)
* Experience in Customer-focused Laboratory Environment (Preferred)
Target Pay Range: $40-48/hour
*
* Your Benefits:

*** Medical, Dental, Vision
* Flexible Spending & HSA Options
* Life Insurance, Short & Long Term Disability
* Pet Insurance
* 401K Founded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 13 sites across three continents. With a team of more than 3,800 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…
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