KVK Tech, Inc. Jobs Hiring Now

INTRODUCTION

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 ensures deviations, investigations, and quality documentation are accurate, compliant, and aligned with cGMP and regulatory requirements. The ideal candidate will demonstrate strong technical writing skills, experience owning deviations and CAPAs, and the ability to collaborate cross-functionally to support compliant manufacturing and continuous improvement.

ROLE AND RESPONSIBILITIES

This position’s responsibilities will include, but not be limited to the following:

• Investigate and document quality events including deviations, incidents, planned deviations, OOS investigations, and customer complaints.
• Perform and document root cause analyses and develop appropriate corrective and preventive actions (CAPAs) in alignment with regulatory expectations.
• Draft, revise, and maintain controlled documentation such as SOPs, batch records, qualification and validation protocols, technical reports, and risk assessments.
• Support change control activities related to manufacturing processes, equipment, facilities, and quality systems.
• Collaborate with Manufacturing, Packaging, Engineering, and Quality teams to ensure documentation accuracy and procedural alignment.
• Support continuous improvement initiatives through trend analysis, audit observations, and quality system enhancements.

BASIC QUALIFICATIONS

• Bachelor’s degree in a scientific or technical discipline such as Chemistry, Biology, Pharmacy, or Engineering required; Master’s degree preferred.
• Minimum 3–5+ years of experience in a pharmaceutical or regulated manufacturing environment.
• Demonstrated experience in technical writing, deviation and CAPA management, and change control systems.
• Working knowledge of cGMP requirements (21 CFR Parts 210/211) and FDA quality system expectations.
• Strong written communication, analytical, and organizational skills with a high attention to detail.

PREFERRED QUALIFICATIONS

What We Offer

• 401(k) with company match
• Health, vision, and dental Insurance
• Childcare expense reimbursement
• Tuition reimbursement
• Annual bonus eligibility
• Annual merit increases
• Paid Time Off and Flexible Holidays

KVK Tech is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status. We encourage you to apply if you feel that you are a match! We look forward to hearing from you. Apply for this position.