KVK Tech is seeking an experienced Packaging Line Leader to join our team in Newtown, PA. The Packaging Line Leader serves as a hands-on working lead responsible for coordinating daily packaging line operations in support of oral solid dosage pharmaceutical manufacturing. This role ensures packaging activities are performed in accordance with cGMP requirements, SOPs, and […]
Posts By: KVK HR
Procurement Associate
KVK Tech is seeking a detail-oriented Procurement Associate to join our team in Newtown, PA. The Procurement Associate will support the sourcing and purchasing of materials, equipment, and services essential to pharmaceutical manufacturing and business operations. This role ensures procurement activities are executed in compliance with company procedures, cGMP requirements, and approved supplier programs while […]
Mechanic
KVK Tech is seeking a skilled and reliable Mechanic to join our team in Newtown, PA. The Mechanic will perform mechanical maintenance, troubleshooting, and equipment changeovers in support of pharmaceutical manufacturing operations. This role is critical to maintaining equipment reliability, minimizing downtime, and ensuring compliance with cGMP, FDA, and safety requirements. The ideal candidate will […]
Accounts Payable Specialist
KVK Tech is seeking an Accounts Payable Specialist to join our team in Newtown, PA. The Accounts Payable Specialist is responsible for managing the day-to-day accounts payable operations within a dynamic pharmaceutical manufacturing organization. This role focuses primarily on the accurate and timely processing of vendor invoices and payments while ensuring compliance with internal controls, […]
QA Investigations / Technical Writer
KVK Tech is seeking an experienced QA Investigations / Technical Writer to join our team in Newtown, PA. The QA Investigations / Technical Writer is responsible for supporting site quality systems through the investigation of quality events and the development, review, and maintenance of controlled documentation within an oral solid dosage manufacturing environment. This role […]
QA Batch Record Reviewer – 2nd Shift
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, […]
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 […]
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