Quality Validation Engineer

Astrix; Roanoke (VA); On-site; USD 46,838 - 53,037; Full time

Job summary

A leading manufacturer of personal care products is seeking a Quality Validation Engineer in Roanoke, VA. This role will support validation and compliance activities within a regulated manufacturing environment, focusing on ensuring adherence to cGMP regulations. Responsibilities include developing validation protocols, maintaining documentation, and collaborating with engineering and quality teams. The ideal candidate will have a Bachelor's degree in Mechanical or Chemical Engineering and 1-3 years of relevant experience. Strong communication skills are essential for this onsite position.

Qualifications

• Bachelor’s degree required in engineering or related technical field.
• 1-3 years of validation experience in a cGMP manufacturing environment preferred.
• Experience with validation of processes and equipment is a plus.

Responsibilities

• Develop and execute validation protocols for equipment and processes.
• Prepare and maintain validation documentation and SOPs.
• Support validation activities for systems and equipment.

Skills

Process validation

Equipment validation

Cleaning validation

Utility validation

Collaboration

Communication

Technical documentation

Education

Bachelor’s degree in Mechanical Engineering

Bachelor’s degree in Chemical Engineering

Related technical field

Tools

Microsoft Office

Technical documentation tools

Job description

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