Regulatory QA Document Control Specialist
Swiss American CDMO, LLC.
Swiss American CDMO, LLC. is seeking a Document Control Specialist to ensure QA documentation aligns with FDA/ISO standards and GMP requirements. The role involves reviewing batch records, handling ERP/MRP entries, scanning records into Laserfiche, and maintaining Product Master Files. You will work on-site five days a week, supporting audits, CAPA, and cross-training with QA peers to sustain compliant documentation processes across materials and finished goods. #J-18808-Ljbffr Swiss American CDMO, LLC.
Vacancy posted 4 days ago
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