KVK Tech is seeking a detail-oriented Weighing & Blending Operator to join our team in Newtown, PA. The Weighing & Blending Operator will perform the weighing, dispensing, staging, and blending of raw materials used in oral solid dosage (OSD) manufacturing. This position requires the ability to follow approved Master Batch Records, accurately handle and reconcile […]
Posts By: KVK HR
Assistant Manager, Packaging
KVK Tech is seeking an experienced Assistant Manager, Packaging to join our team in Newtown, PA. The Assistant Manager, Packaging will support the Packaging Manager in leading daily packaging operations within a regulated oral solid dosage pharmaceutical manufacturing environment. This role provides operational leadership across packaging lines, shifts, and personnel to ensure production schedules are […]
QA Inspector – 1st 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 […]
Manufacturing Supervisor (1st & 2nd Shift)
KVK Tech is seeking an experienced Manufacturing Group Lead to join our team in Newtown, PA. The Manufacturing Supervisor is responsible for overseeing daily oral solid dosage manufacturing operations to ensure production activities are executed safely, efficiently, and in compliance with cGMP requirements, approved procedures, and established production schedules. This role provides direct leadership to […]
Manufacturing Group Lead (1st & 2nd Shift)
KVK Tech is seeking an experienced Manufacturing Group Lead to join our team in Newtown, PA. The Manufacturing Group Lead serves as a hands-on, working lead responsible for supporting daily oral solid dosage manufacturing operations across areas such as weighing, blending, compression, coating, encapsulation, and related processes. This role provides rotating room coverage, directs floor […]
Packaging Supervisor (3:30 pm-12:00 am)
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 […]
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, […]
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 […]
Recent Comments