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 […]
Posts By: KVK HR
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, […]
GMP Compliance Video Reviewer
KVK Tech is seeking a detail-oriented GMP Compliance Video Reviewer to join our Quality Assurance team in Newtown, PA. The GMP Compliance Video Reviewer provides independent QA oversight through the review of recorded manufacturing and packaging video footage to verify compliance with approved batch records, SOPs, and cGMP requirements. This role plays a critical part […]
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. […]
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, […]
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 […]
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 […]
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, […]
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