KVK Tech, Inc.
A leading pharmaceutical company in Newtown, PA is seeking a Documentation Associate to support Quality Control operations. The role involves preparing and maintaining analytical methods, managing documentation compliance, and collaborating with QC personnel. Ideal candidates will have an associate's degree in a scientific discipline, plus 1–2 years' experience in a GMP-regulated environment. Comprehensive benefits include a 401(k) plan, healthcare, and tuition reimbursement.
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