KVK Tech is seeking a Cleaning Technician to join our team in Newtown, PA. The Cleaning Technician supports pharmaceutical manufacturing and packaging operations by ensuring production equipment and controlled manufacturing areas are thoroughly cleaned and maintained in accordance with current Good Manufacturing Practices (cGMP). This role is responsible for disassembling, cleaning, and reassembling production equipment… Read more »
Posts By: KVK HR
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… Read more »
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… Read more »
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… Read more »
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… Read more »
Packaging Operator – 2nd Shift
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,… Read more »
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… Read more »
Senior HR Associate
KVK Tech is seeking a Senior HR Associate to join our team in Newtown, PA. The Senior HR Associate will support day-to-day HR operations while leading key functional areas including recruitment, onboarding, employee relations support, HR compliance, and personnel documentation. This role ensures timely, accurate, and regulation-compliant HR service delivery aligned with federal/state employment laws… Read more »
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…. Read more »
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,… Read more »
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