QC Documentation Specialist: ALCOA+ & cGMP
KVK Tech, Inc.
KVK Tech, Inc. in Newtown, PA seeks a QC Documentation Associate to manage analytical methods, specs, controlled spreadsheets, and Empower calculations. The role emphasizes ALCOA+ data integrity and inspection-ready records in a GMP setting. Ideal candidates have 0–3 years in a GMP pharmaceutical environment with strong Word/Excel skills and familiarity with USP/NF, EP, and JP. This is an on-site position offering growth in QC documentation practices. #J-18808-Ljbffr KVK Tech, Inc.
Vacancy posted 1 day ago
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