QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

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We are seeking a Validation Specialist to support validation activities within the Injection Molding area. The selected candidate will assist in the execution, documentation, and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requirements.

Key Responsibilities

• Support the execution of validation protocols for Molding processes and equipment.
• Collect, analyze, and document validation data and results.
• Collaborate with Manufacturing, Engineering, Quality, and Validation teams to ensure project objectives are met.
• Assist in the investigation and resolution of validation-related issues, deviations, and corrective actions.
• Maintain accurate documentation in compliance with cGMP requirements and internal procedures.
• Participate in continuous improvement initiatives and provide technical support as needed.
• Ensure assigned activities are completed within established timelines and quality standards.

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field.
• Previous experience in validation activities within a regulated environment preferred (Medical Device, Pharmaceutical, or Manufacturing).

All your information will be kept confidential according to EEO guidelines.