KVK Tech is seeking a reliable Packaging Operator I to join our team in Newtown, PA. The Packaging Operator I supports routine packaging operations for oral solid dosage pharmaceutical products in a regulated manufacturing environment. This role is responsible for operating packaging equipment, performing in-process checks, and maintaining accurate documentation to ensure product quality, safety,… Read more »
Posts By: KVK HR
QA Inspector – 2nd Shift
KVK Tech is seeking a dedicated QA Monitor to join our team in Newtown, PA. The QA Inspector provides real-time oversight on the manufacturing and packaging floors to ensure products meet cGMP requirements, internal quality standards, and applicable regulatory expectations. This role is essential in supporting in-process inspections, documentation review, and deviation identification, helping maintain… Read more »
Senior HR Associate
KVK Tech is seeking a Senior HR Associate to join our team in Newtown, PA. The Senior HR Associate will support day-to-day HR operations while leading key functional areas including recruitment, onboarding, employee relations support, HR compliance, and personnel documentation. This role ensures timely, accurate, and regulation-compliant HR service delivery aligned with federal/state employment laws… Read more »
Microbiologist I
KVK Tech is seeking a Microbiologist I to join our team in Newtown, PA. The Microbiologist I will perform routine microbiological testing and environmental monitoring in support of sterile and oral solid dosage manufacturing. This role ensures testing is performed in compliance with cGMP and data integrity principles to maintain product quality and contamination control…. Read more »
QC Chemist I
KVK Tech is seeking a QC Chemist I to join our team in Newtown, PA. The QC Chemist I will perform routine analytical testing to support the release of raw materials, packaging components, in-process samples, finished products, and stability studies in a cGMP-regulated environment. This role operates laboratory instrumentation, executes validated and compendial analytical methods,… Read more »
Documentation Associate
KVK Tech is seeking a Documentation Associate to join our team in Newtown, PA. The Documentation Associate will support Quality Control operations by maintaining accurate, complete, and compliant documentation across the analytical data lifecycle. This role ensures analytical methods, specifications, controlled spreadsheets, and Empower calculations are properly created, updated, versioned, and archived in accordance with… Read more »
QA Chemist
KVK Tech is seeking a QA Chemist to join our team in Newtown, PA. The QA Chemist will ensure the accuracy, completeness, and regulatory compliance of analytical laboratory data through systematic, scientifically sound review practices. This role verifies adherence to test methods, SOPs, specifications, validation requirements, and cGMP/data integrity standards while identifying discrepancies, trends, and… Read more »
AR&D Manager
KVK Tech is seeking an AR&D Manager to join our team in Newtown, PA. The AR&D Manager will provide strategic, technical, and operational leadership for all Analytical Research & Development laboratory functions supporting product development, stability programs, raw materials, intermediates, and finished products. This role oversees analytical method development, validation, transfer, troubleshooting, and compliance activities,… Read more »
Analytical Chemist I
KVK Tech is seeking an Analytical Chemist I to join our team in Newtown, PA. The Analytical Chemist I will perform analytical testing to support product development, validation, and routine quality operations within a cGMP-regulated laboratory environment. This role operates analytical instrumentation—including HPLC/UPLC, GC, UV-Vis, and dissolution systems—while maintaining rigorous documentation, data integrity, and adherence… Read more »
Senior QA Associate
KVK Tech is seeking a Senior QA Associate to join our team in Newtown, PA. The Senior QA Associate will serve as a key Quality Systems subject matter expert (SME), supporting multiple core elements of the site Quality Management System (QMS), including deviations, investigations, CAPAs, change controls, complaints, document control, and quality event trending. This… Read more »
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