Siegfried · 2 days ago
Quality Control Raw Materials Associate II (2nd Shift)
Irvine, CA
Full-time
Onsite
Mid Level
$27/hr - $30/hr
3+ years expSiegfried is a global company and trusted partner to the pharmaceutical industry, committed to safety, quality, and sustainability. They are seeking a Quality Control Associate II to support raw material inspection, testing, and release, while collaborating with various departments to ensure compliance with internal specifications and regulatory requirements.
BiotechnologyHealth CareManufacturingMedicalPharmaceutical
Responsibilities
Independently execute QC inspection and testing to support routine manufacturing activities and new clinical/development products
Perform sampling of raw materials for chemistry and microbiology testing in clean room classified areas, minimizing contamination using aseptic technique
Collaborate with tech transfer teams to design raw material specifications for new materials and improve specifications for existing materials
Become proficient in use of Labware LIMS 8
Perform inspection in compliance with relevant regulations
All activities are performed in GMP/GDP environment
Support and participate in internal and external audits, including direct interaction with auditors when discussing raw material inspection processes and records
Collaborate with purchasing, QA and the supplier to resolve issues with nonconforming batches of raw materials
Attend production and project meetings as representative of QCRM group to communicate status updates on pending raw material release
Maintain the working areas in a clean and organized state
Assist in Quality oversight of warehouse operations
Any and all other duties assigned by immediate supervisor
Qualification
Required
Knowledge of quality systems, FDA and compendium requirements
Familiarity with ANSI/ASQ sampling plans
Ability to sample aseptically, perform fine measurements using tools and learn new instrumentation
Advanced written/oral communication skills and advanced computer skills
Capable of using good reason and judgment to make and defend recommendations
Positive team player in a fast-paced environment
B.S. in Chemistry, Biology or other Pharmaceutical-relevant degree
3+ years of Experience in QC or QA
3+ years of Experience in FDA Regulated industry
Preferred
Experience performing Raw Material Inspection
Benefits
Medical, Dental, Vision, Life Insurance
FSA/HSA
Voluntary Accident, Critical, Hospital, Pet
401K
Company
Siegfried
Siegfried is a leading CDMO with 13 production sites on three continents.
1001-5000 employees
H1B Sponsorship
Siegfried has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2020 (1)
Funding
Current Stage
Public CompanyTotal Funding
unknown1995-04-07IPO
Leadership Team
Marcel Imwinkelried
CEO
Reto Suter
CFO
Recent News
2025-09-10
2025-08-21
Company data provided by crunchbase