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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The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. This role ensures compliance with cGMP regulations through the planning, execution, and documentation of validation activities for analytical instruments, with a strong focus on UPLC systems and densitometer. The specialist will support laboratory operations by maintaining validated states and ensuring data integrity and regulatory

• Bachelor’s degree in Science, or a related scientific discipline.
• Minimum of three (3) years of relevant experience in a regulated laboratory in pharmaceutical environment.
• Demonstrated hands‑on experience in the validation of UPLC systems and densitometer.
• Strong knowledge of equipment qualification and validation requirements, data integrity principles, and applicable regulatory expectations.
• Bilingual in English and Spanish (written and spoken).
• Excellent technical writing, organizational, and communication skills.

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