Randstad
Job Location :
Myerstown,PA, USA
Posted on :
2025-08-20T05:09:01Z
Job Description :
\n\n\n\t. Review test results, in-process records, and QA documentation for compliance with specifications.\n\t. Audit manufacturing and packaging documentation for accuracy and adherence to cGMP standards.\n\t. Coordinate with QA, Supply Chain, Production, and Supplier Quality to support timely product release.\n\t. Maintain and update databases including supplier approvals, release charts, and deviation reports.\n\t. Support investigations with batch record reviews, calculations, and data verification.\n\t. Write, revise, and maintain SOPs and QA documentation.\n\n\n. Qualifications\n\n\n\t. High School Diploma or GED with at least 3-5 years of document review/auditing experience in a cGMP-regulated industry.\n\t. PC skills; proficiency with Microsoft Office required.\n\t. Experience with SAP, MES, or other automated inventory systems strongly preferred.\n\n\n. Perks of the Role\n\n\n\t. Competitive pay at $35.50/hr.\n\t. Full-time, consistent schedule (day shift, Monday-Friday).\n\t...QA, Assistant, High School, Technology, Staffing
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