Job Information
Astrix Technology Quality Validation Engineer in Roanoke, Virginia
Quality Validation Engineer
Quality Assurance
Roanoke, Virginia, US
- Added - 10/03/2026
Pay Rate Low: 34 | Pay Rate High: 38.50
Pay Rate Low: 34 | Pay Rate High: 38.50
A 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
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We 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.