Validation Engineer

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Location:

Greenville/Liberty Pay:

$35-44/hour

Duration:

6 months- Potential to Convert Currently seeking a Validation Engineer to support an increased volume of medical manufacturing work at our Liberty, SC location. This role will focus on executing validation and qualification activities for custom-engineered automation solutions supporting medical and process manufacturing customers. The individual in this role will be responsible for executing test scripts, supporting commissioning and qualification activities, and ensuring compliance with applicable validation standards. This position will work closely with engineering, controls, and project teams and will take direction from the project lead.

Summary of role:

Provide validation experience and guidance during equipment design, software design, build, debug, and qualification phases of a project. Develop pertinent document templates tailored to customer SOP's. Write overall project quality (validation scope) plans. Organize, guide, and write requirement specifications as necessary. Organize, guide, and write qualification plans and protocols as necessary. Review qualification/requalification packages for completeness and accuracy, sound rationale, compliance with validation policies. Interface with internal and client validation and engineering teams to secure document approvals. Oversee and execute validation qualifications at our facility and at the customer's site. Create validation summary reports. Drive a quality approach into the organization, change control, and documentation for the equipment design, software, and documentation. Support all aspects of the Validation life cycle, from design through operation and improvement Key Responsibilities Execute validation and qualification activities in a GAMP 5-based validation model Execute approved test scripts and support commissioning and qualification of equipment Support validation of custom-engineered automation systems, including multiple pieces of equipment on a single customer program Review and work from electrical design drawings Support development and execution of validation documentation, including IQ/OQ activities Assist with debugging and troubleshooting of custom machines during commissioning Collaborate effectively within a cross‑functional engineering team environment Communicate validation progress, issues, and risks effectively to project stakeholders Demonstrate strong documentation, organization, and presentation skills Mentor and support project team members through validation activities without direct authority Required Qualifications Bachelor's degree (required) in: Systems Engineering, Life Sciences, Electrical Engineering or related technical discipline. 3+ years of experience performing validation activities Experience working within process and validation environments Proficiency with Microsoft Office Strong ability to work independently with minimal guidance Demonstrated experience working in a team-based environment Excellent communication and presentation skills Preferred Qualifications Experience with custom-engineered automation solutions Background in Medical Devices, Life Sciences, pharmaceutical, or food manufacturing Experience commissioning and qualifying multiple pieces of equipment Experience with packaging systems and/or vision systems Experience developing or executing design qualification (DQ/ IQ/ OQ) documentation Familiarity with Rockwell Automation PLC control systems Hands-on experience debugging or supporting custom machine builds  HRU is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Apply for this job Copy link ✓ Thanks for sharing! Find any service AddToAny More…