Quality Control Associate Ii – Raw Material Inspection (2nd Shift)

Siegfried

Base: $30-32ph; bonus/equity: not specified; benef...
2nd shift (2:00 pm - 10:30 pm)
Bachelor's degree in chemistry or biology
3 years qc/qa experience in fda-regulated industry
Aseptic sampling techniques in cleanroom environments
Siegfried is seeking a Quality Control Associate II for Raw Material Inspection on the 2nd Shift, who will support the inspection, testing, and release of raw materials in a pharmaceutical manufacturing environment. The ideal candidate will have a degree in a relevant scientific field and a minimum of three years of experience in quality control within an FDA-regulated industry

Job Summary

  • This role supports the receipt, inspection, sampling, and release of raw materials used in the manufacture of sterile drug products within a GMP-regulated environment.
  • The position requires independent execution of physical testing activities using laboratory instrumentation and adherence to strict aseptic techniques during cleanroom sampling.
  • Siegfried offers competitive compensation including a shift differential for 2nd shift work along with comprehensive benefits such as medical, dental, vision, and 401K.

Matching Summary

Match Score: 85

Siegfried is seeking a Quality Control Associate II for Raw Material Inspection on the 2nd Shift, who will support the inspection, testing, and release of raw materials in a pharmaceutical manufacturing environment. The ideal candidate will have a degree in a relevant scientific field and a minimum of three years of experience in quality control within an FDA-regulated industry.

Salary

Base: $30-32/hour; Bonus/Equity: Not specified; Benefits: +10% Shift Differential for 2nd Shift

Skills & Requirements

Must-have

  • Bachelor's degree in Chemistry or Biology
  • 3 years QC/QA experience in FDA-regulated industry
  • Aseptic sampling techniques in cleanroom environments
  • Knowledge of FDA and compendial requirements
  • Experience with Labware LIMS 8
  • Familiarity with ANSI/ASQ sampling plans

Nice-to-have

  • Experience in pharmaceutical raw material inspection
  • Cross-functional collaboration skills
  • Strong analytical thinking and judgment
  • Participation in internal and external audits
  • Ability to work in fast-paced team environment

Key Requirements

  • Bachelor's degree in Chemistry, Biology, or relevant field
  • Minimum 3 years QC or QA experience in FDA-regulated industry
  • Working knowledge of quality systems and regulatory expectations

Work Rights

Not specified

Tailored Resume

Cover Letter