Quality Validation Engineer

**Quality Validation Engineer**Quality AssuranceRoanoke, Virginia, US+ Added - 10/03/2026Pay Rate Low: 34 | Pay Rate High: 38.50Pay Rate Low: 34 | Pay Rate High: 38.50A leading manufacturer of **beauty, personal care, and home care products** is seeking a **Quality Validation Engineer** to support validation and compliance activities within a regulated manufacturing environment. This role is responsible for planning, executing, and documenting validation activities to ensure compliance with **cGMP regulations and internal quality standards** .**Location:** Roanoke, VA**Schedule:** Monday - Friday | Day Shift**Contract (6 months to start)****100% onsite****Key Responsibilities**+ Develop, review, and execute **validation protocols (IQ/OQ/PQ)** for equipment, processes, cleaning procedures, and utility systems+ Prepare and maintain **validation documentation, reports, and SOPs** to ensure compliance and audit readiness+ Support validation activities for systems such as **USP water systems, compressed air, and manufacturing equipment**+ Collaborate with **Engineering, Quality Assurance, and Operations** on validation requirements and system qualifications+ Assist with **environmental monitoring activities** and coordinate with third-party laboratories when needed+ Participate in **internal and external audits** and provide documentation and technical support during inspections+ Support **deviations, investigations, and root cause analysis** related to validation or equipment issues+ Provide validation input for **equipment purchases, process changes, and system improvements**+ Participate in cross-functional meetings to provide **technical guidance on validation and compliance requirements****Qualifications****Education**+ Bachelor's degree in Mechanical Engineering, Chemical Engineering, or related technical field required**Experience**+ 1-3 years of validation experience in a cGMP manufacturing environment preferred+ Experience validating processes, equipment, instrumentation, or computer-controlled systems preferred+ Industry experience in cosmetics, pharmaceutical, personal care, or regulated manufacturing is a plus**Skills**+ Strong knowledge of process, equipment, cleaning, and utility validation+ Experience developing and executing IQ/OQ/PQ protocols+ Familiarity with cGMP compliance and regulatory requirements+ Ability to write and maintain technical documentation and SOPs+ Experience supporting investigations, deviations, and root cause analysis+ Strong collaboration and communication skills across engineering, quality, and operations teams+ Proficiency with Microsoft Office and technical documentation tools\#LI-CS1INDBHWe are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.