Siegfried
pharmaceutical
QualityControlAssociateII–RawMaterialInspection(2ndShift)
Neural analysis suggests this role is
optimal for Mid candidates.
“Quality Control Associate II – Raw Material Inspection (2nd Shift) at Siegfried. Skills: Raw material inspection, Physical testing, Sampling. Execute QC inspection and physical testing. Perform sampling of raw materials”
What You'll Achieve.
ensure materials meet specifications; released in a timely manner
Industry & Context.
analytical thinking and judgment; ability to make and defend recommendations
2nd Shift (2:00 PM - 10:30 PM), hands-on laboratory and cleanroom work, sampling of raw materials in classified environments, use of appropriate personal protective equipment
What They're Looking For.
Must Have
Bachelor’s degree in Chemistry, Biology, or other pharmaceutical-relevant scientific discipline, Minimum of 3 years of experience in QC or QA within an FDA-regulated industry, Working knowledge of quality systems and regulatory expectations including FDA and compendial requirements, Familiarity with ANSI/ASQ sampling plans, Ability to perform aseptic sampling, use precision measurement tools, and learn new laboratory instrumentation, written and verbal communication skills with effective documentation practices in a GMP environment, analytical thinking and judgment with the ability to make and defend recommendations, Ability to work effectively in a fast-paced, cross-functional team environment
Nice to Have
Experience performing raw material inspection in a GMP-regulated pharmaceutical or biotechnology environment
What You'll Do.
Execute QC inspection and physical testing
Perform sampling of raw materials
Support development of raw material specifications
Perform inspection activities
Resolve issues related to nonconforming raw material lots
Attend production and project meetings
Maintain laboratory and sampling areas
How You'll Work.
Team & Collaboration
Collaborates cross-functionally with Chemistry, Microbiology, Engineering, Purchasing, Warehouse, and Quality Assurance; Support development and improvement of raw material specifications in Labware LIMS 8 in collaboration with cross-functional teams; Collaborate with Purchasing, QA, and suppliers to resolve issues related to nonconforming raw material lots; Attend production and project meetings to provide updates
Communication Scope
written and verbal communication skills; effective documentation practices
Full Job Description
"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, Raw Materials - 2nd Shift (2:00 PM - 10:30 PM) The Quality Control Associate II (Raw Material Inspection), 2nd Shift is an individual contributor within the QC Raw Materials team responsible for supporting raw material receipt, inspection, sampling, physical testing, and release of materials used in the manufacture of sterile drug products. The role supports development, revision, and maintenance of raw material specifications within Labware LIMS 8, ensuring alignment with compendial and regulatory requirements. The position also supports quality investigations such as deviations, OOS, and vendor corrective actions. This role includes hands-on sampling of bulk materials in classified cleanroom environments, physical testing using laboratory instrumentation, and dimensional inspection of components. The associate collaborates cross-functionally with Chemistry, Microbiology, Engineering, Purchasing, Warehouse, and Quality Assurance to ensure materials meet specifications and are released in a timely manner. **Your Profile:** **Key Responsibilities** * Independently execute QC inspection and physical testing activities to support routine manufacturing and development programs. * Perform sampling of raw materials for chemistry and microbiology testing in cleanroom classified areas using appropriate aseptic techniques to mini
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