KVK Tech is seeking a 2nd Shift QA Batch Record Reviewer to join our team in Newtown, PA. The QA Batch Record Reviewer is responsible for reviewing executed packaging batch documentation to ensure accuracy, completeness, and compliance with cGMP requirements and internal quality standards. This role plays a critical part in supporting compliant batch documentation, […]
Posts By: KVK HR
Packaging Operator – 2nd Shift (3:30p-12:00a)
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, […]
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 […]
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. […]
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 […]
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 […]
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 […]
QA Monitor – 2nd Shift
KVK Tech is seeking a detail-oriented QA Monitor to join our team in Newtown, PA. The QA Monitor plays a critical role in ensuring that all cleaning, sanitation, and line clearance activities are performed in strict alignment with cGMP, internal SOPs, and FDA expectations. This position provides continuous on-floor QA oversight to verify equipment readiness, […]
Electrician
KVK Tech is seeking a skilled Electrician to join our team in Newtown, PA. The Electrician will support reliable operation of pharmaceutical manufacturing, packaging, and facility systems by installing, maintaining, troubleshooting, and repairing industrial electrical equipment in compliance with cGMP, NEC, OSHA, and company safety standards. This role ensures safe and continuous operation of power […]
Packaging Mechanic
KVK Tech is seeking a skilled Packaging Mechanic to join our team in Newtown, PA. The Packaging Mechanic will support oral solid dosage (OSD) packaging operations through the setup, adjustment, maintenance, and troubleshooting of automated and semi-automated equipment. This role ensures that packaging lines operate safely, efficiently, and in compliance with cGMP and FDA requirements. […]
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