{"id":1432153,"url":"https://alion.io/job/siegfried-quality-assurance-associate-i-2nd-shift","title":"Quality Assurance Associate I - 2nd Shift","company":{"id":1865765,"name":"Siegfried","domain":"siegfried.ch","url":"https://alion.io/company/siegfried","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":81,"open_postings":9,"ghost_share":0,"stale_share":0.556,"repost_share":0,"time_to_fill_p50_days":64,"computed_at":"2026-11-05T05:54:30Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Irvine, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":30,"max":32,"currency":"USD","period":"hour","gross":null,"usd_annual":64000},"salary_estimate":null,"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CAPA","optional":false},{"name":"GMP","optional":false},{"name":"LIMS","optional":false}],"status":"live","first_seen_at":"2026-07-14T00:00:00Z","employer_posted_date":"2026-07-14","last_verified_at":"2026-11-06T03:35:06Z","board_verified":true,"closed_at":null,"days_open":115,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":115},"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-offeringlong-term opportunities to grow and make an impact.\nYour Role:\nThe QA Associate I supports the Quality Assurance Operation on the 2nd Shift, which consists of QA Production Floor supports, and QA Product Release.2nd Shift Hours: 2 PM - 10:30 PM Monday through Friday\nYour Profile:\nResponsibilities\nQA Production Floor Support\nProvide Quality support to Manufacturing personnel on the shop floor for compounding and QA- in-process checks.\nPerform line clearance verification, sterilization chart review, scale calibration verification, and QA in-process checks including but not limited to visual inspection, CSIT/PID test, weight check, and torque test.\nPerform AQL and Level II Visual Inspection for Finished products.\nPrepare in-process samples for submission to the Quality Control laboratory. Support handling of GMP events and initiation of deviation investigations.\nRead, understand, and follow SOP’s and comply with cGMP and GDP.\nSupport the issuance of GMP documentation to the Manufacturing floor.\nQA Batch Review and Product Release \nReview executed batch records for completeness, accuracy and compliance with approved procedures and Good Documentation Practices (GDP) and resolve discrepancies with manufacturing operators or supervisors.\nUse computerized systems and software such as SAP, LIMS, and TrackWise for data collection and batch record review.\nEnter and verify data from executed batch records into the Product Log Sheet and maintain the database up to date at all times.\nParticipate in deviation investigation and CAPA implementation.\nInitiate Certificate of Conformance and prepare executed batch records for product release in a timely manner to meet compliance requirements and business needs.\nScan and file batch records (physically & electronically).\nAssist in writing and/or revising SOPs to ensure compliance with cGMP and other applicable regulations.\nRequired Knowledge, Skills and Abilities\nWorking knowledge of QA principles In Pharmaceutical and/or other FDA regulated industries required\nGood computer skills\nStrong attention to detail\nGood oral and written communication skills\nAbility to work overtime and/or work\non weekend as needed\nRequired Education and Experience\nBachelor's Degree in Biochemistry, Chemistry, Engineering, Biology or closely related discipline required\n1-2 years' experience in Quality Assurance / Manufacturing environment in Pharmaceutical or other GMP regulated industries required\nTarget Pay Range: $30-32/hour +10% Differential when working on 2nd Shift (2 PM -10:30 PM)\nIndividual compensation packages are based on various factors unique to each candidate, including skill set, experience, qualifications and other job-related reasons.\nYour Benefits:\nMedical, Dental, Vision, Life\nVoluntary Accident, Hospital, Pet\n401K\nGenerous Time Off Structure including PTO, Holidays, Sick & Personal\nFounded in 1873 in Zofingen, Switzerland, Siegfried has grown into a global network of 16 sites across three continents. With a team of more than 4,200 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 APIs and finished dosage forms under one roof. 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