QRC Group, LLC

Principal Engineer with experience:Working with clean utilities systems such as: Distilled Water Purified Water RO System. Experience working on Clean Gases Process Air GMP gasses supply like Oxygen Nitrogen. Experience documenting and managing Deviation non-conformance. Proficient

Principal Engineer with experience:Working with clean utilities systems such as: Distilled Water Purified Water RO System. Experience working on Clean Gases Process Air GMP gasses supply like Oxygen Nitrogen. Experience documenting and managing Deviation non-conformance. Proficient

Industrial Engineer with experience in regulated industry.RESPONSABILITIES:Lead Lean Manufacturing initiatives focused on waste elimination across the site including but not limited to: Value stream mapping change-over optimization (SMED) and Time studiesStandard work development for

Industrial Engineer with experience in regulated industry.RESPONSABILITIES:Lead Lean Manufacturing initiatives focused on waste elimination across the site including but not limited to: Value stream mapping change-over optimization (SMED) and Time studiesStandard work development for

The Project Coordinator supports the SAP implementation at the Puerto Rico site by acting as the primary link between the D&T ERP/SAP teams and local business users. The role includes coordinating project activities managing communication assisting with requirement gathering and DevOp

The Project Coordinator supports the SAP implementation at the Puerto Rico site by acting as the primary link between the D&T ERP/SAP teams and local business users. The role includes coordinating project activities managing communication assisting with requirement gathering and DevOp

Sr Associate Tech Engineering with knowledge on: Mechanical equipment adjustment/troubleshooting. PLC Systems troubleshooting-RockwellVision Systems troubleshooting/adjustment-CognexcGMPs Systech vision systemsFDA regulation Basic control systems hardwareRequirementsMasters Degree or

Sr Associate Tech Engineering with knowledge on: Mechanical equipment adjustment/troubleshooting. PLC Systems troubleshooting-RockwellVision Systems troubleshooting/adjustment-CognexcGMPs Systech vision systemsFDA regulation Basic control systems hardwareRequirementsMasters Degree or

Sr Validation Scientist with experience in Parenteral Manufacturing. Specifically experience focused on Aseptic Process Validation Aseptic Techniques Environmental Monitoring Performance Qualifications Environmental Characterizations Airflow Visualization (Smoke Tests). Experience wri

Sr Validation Scientist with experience in Parenteral Manufacturing. Specifically experience focused on Aseptic Process Validation Aseptic Techniques Environmental Monitoring Performance Qualifications Environmental Characterizations Airflow Visualization (Smoke Tests). Experience wri

Responsible for providing quality leadership governance and expertise in Quality Assurance processes related to the manufacture. Ensure compliance with regulatory requirements and West procedures. Proactively develop lead and drive the execution of the Quality Assurance strategy. Deve

Responsible for providing quality leadership governance and expertise in Quality Assurance processes related to the manufacture. Ensure compliance with regulatory requirements and West procedures. Proactively develop lead and drive the execution of the Quality Assurance strategy. Deve

QRC Group is a leading provider of consulting engineering validation quality and talent solutions for the pharmaceutical biotechnology and regulated manufacturing industries. Our mission is to connect top-tier talent with essential projects that drive innovation quality and operationa

QRC Group is a leading provider of consulting engineering validation quality and talent solutions for the pharmaceutical biotechnology and regulated manufacturing industries. Our mission is to connect top-tier talent with essential projects that drive innovation quality and operationa

Validation Engineer with experience in automated equipment and vision system validation (protocol generation execution and reporting). Experience in generating manufacturing procedures and preventive maintenance. Strong knowledge generating validation documents: Installation and Opera

Validation Engineer with experience in automated equipment and vision system validation (protocol generation execution and reporting). Experience in generating manufacturing procedures and preventive maintenance. Strong knowledge generating validation documents: Installation and Opera

Junior Automation Engineer to support the development improvement and maintenance of automated production systems. This role contributes to enhancing product quality operational efficiency and safety while assisting engineering projects equipment upgrades and facility modifications. D

Junior Automation Engineer to support the development improvement and maintenance of automated production systems. This role contributes to enhancing product quality operational efficiency and safety while assisting engineering projects equipment upgrades and facility modifications. D

Software Application Configuration Specialist to integrate their expertise in the implementation of TULIP System. Background in industries such as Medical Devices & Pharma. Responsibilities: Contribute to practice goals and continuous improvement initiatives technology. Engage in bus

Software Application Configuration Specialist to integrate their expertise in the implementation of TULIP System. Background in industries such as Medical Devices & Pharma. Responsibilities: Contribute to practice goals and continuous improvement initiatives technology. Engage in bus

Coder / Configurator/ ProgrammerSummary:Responsible for configuration and simulation on Checklist Manager application (prototypes and reports). Must have knowledge of databases and the SQL language (for reports thats critical) and experience in the pharmaceutical industry.Requirements

Coder / Configurator/ ProgrammerSummary:Responsible for configuration and simulation on Checklist Manager application (prototypes and reports). Must have knowledge of databases and the SQL language (for reports thats critical) and experience in the pharmaceutical industry.Requirements

The EHS Coordinator is responsible for implementing maintaining and improving health safety and environmental programs within a medical device manufacturing facility. This role focuses on safe management of hazardous waste compliance with federal and local regulations (OSHA EPA) and a

The EHS Coordinator is responsible for implementing maintaining and improving health safety and environmental programs within a medical device manufacturing facility. This role focuses on safe management of hazardous waste compliance with federal and local regulations (OSHA EPA) and a