KVK Tech is seeking an experienced Packaging Supervisor to join our team in Newtown, PA. The Packaging Supervisor will oversee daily packaging operations within a regulated pharmaceutical manufacturing environment, ensuring activities are executed safely, efficiently, and in compliance with cGMP and regulatory requirements. This role is responsible for leading packaging personnel, maintaining production schedules, ensuring […]
Posts By: KVK HR
Packaging Line Leader (3:30 pm – 12:00 am)
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 […]
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, […]
Analytical Chemist II
KVK Tech is seeking an experienced Analytical Chemist II to join our team in Newtown, PA. The Analytical Chemist II will independently perform analytical testing and support method development, validation, and technical transfer activities for oral solid dosage pharmaceutical products. This role plays a critical part in ensuring data integrity, regulatory compliance, and high-quality analytical […]
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, […]
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 […]
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