Company 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…
Company 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…
Company 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…
Company 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…
Company 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…
Company 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…
Company 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…
Validation Specialist with experience in regulated industry validating/qualifying manufacturing equipment and processes. Tasks Execute complete validation cycle Perform IQ/OQ, PQ Manufacturing equipment qualification Process validation Knowledge in CSV Requirements Bachelor in Engineering or Sciences At least three years of experience…
Company 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…
Company 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…
Company 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…
The Validation Manager is responsible for overseeing and managing all validation activities within the pharmaceutical manufacturing facility. This includes equipment, utilities, processes, cleaning, and computerized systems to ensure compliance with regulatory requirements (FDA, EMA, ICH) and company standards. The role…
Company 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…
Company 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…
Validation Specialist with hands on experience in executing validation and qualification activities across diverse areas, including: Process Packaging Manufacturing Laboratory Computer System Validation (CSV) Software Facilities and Utilities Site Acceptance Testing (SAT) & Factory Acceptance Testing (FAT) Commissioning and Decommissioning…
CSV Specialist to support the installation of several manufacturing solid dosage equipment such as but not limited to: Encapsulator Checkweigher Compression machine Hardness tester Encapsulation machine Auxiliary equipment Main activities should include: Verification of the equipment installed and configured at…
Project Specialist will be required to lead, support, and/or manage selected manufacturing projects, which may include process/equipment optimization, business continuity, supplier changes, cost reduction, and sustainability initiatives, among others. Duties & Responsibilities: Identify, lead, support and manage manufacturing improvement projects…
To support the process control activities for the 1st, 2nd and 3rd shift. Support includes, but not limited to the following activities: Process controls and equipment/system troubleshooting. Backup and restore process of systems software. Access control management. Support projects related…
The Validation Manager is responsible for overseeing and managing all validation activities within the pharmaceutical manufacturing facility. This includes equipment, utilities, processes, cleaning, and computerized systems to ensure compliance with regulatory requirements (FDA, EMA, ICH) and company standards. The role…
Process Development Scientist provide direct support to the requirement, design, and characterization of inspection/packaging process, process optimization strategies and/or troubleshooting of operational issues in the operations. Apply advanced and diverse engineering principles to the design and implementation of system, equipment…
Associate Tech Engineering with experience with pneumatics, automatic control and vision inspection systems required.Duties: Identify, and resolve, all problems related to the process equipment and where possible minimize equipment downtime. Complete advanced maintenance activities, including but not limited to preventive…