Job Description

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

Log on now to our website http://www. qrcgroup.com to learn more about our services and solutions!

We are seeking a C&Q Specialist responsible for executing and documenting Installation Qualification (IQ) and Operational Qualification (OQ) activities.

Project Scope

The C&Q activities will support a capital upgrade project that includes:

• Removal and decommissioning of existing equipment, and installation of new equipment.
• Upgrade of the control system and safety architecture.
• Execution of functional and safety testing to confirm proper operation following the upgrade.
• FAT
• CAPA
• Data Integrity

Key Responsibilities

• Provide on-site validation support during shutdown and installation activities
• Execute IQ and OQ protocols and associated components.

• Verify proper installation, configuration, and functionality

• Support and witness functional testing and integrated systems.
• Ensure equipment installation complies with approved drawings, specifications, and manufacturer recommendations.
• Document test results accurately and in compliance with regulated documentation practices
• Identify, document, and support the resolution of deviations, discrepancies, and anomalies
• Generate and complete validation reports and execution summaries.
• Collaborate with related teams during commissioning and qualification activities.
• Ensure all validation activities comply with applicable GxP, safety, and quality requirements

Additional Information

Benefits

What We Offer

• Opportunities for learning, development, and professional growth.
• A collaborative and supportive work environment.
• The opportunity to work with industry-leading clients on impactful projects.

Your information will be kept confidential according to EEO guidelines.