QRC Group, LLC

We are seeking a C&Q Specialist to support a critical shutdown tied to a robotic arm replacement and motion control upgrades (servos/VFDs pneumatic safety interlocks) within a highly automated production system. This role will be responsible for executing and documenting Installation

We are seeking a C&Q Specialist to support a critical shutdown tied to a robotic arm replacement and motion control upgrades (servos/VFDs pneumatic safety interlocks) within a highly automated production system. This role will be responsible for executing and documenting Installation

Chemical analysts with experience in solid dosage analysis and laboratory data review. The role includes performing analyses evaluating results and supporting in the quality control of the laboratory. RequirementsBachelors Degree in Chemistry.Previous laboratory experience in regulate

Chemical analysts with experience in solid dosage analysis and laboratory data review. The role includes performing analyses evaluating results and supporting in the quality control of the laboratory. RequirementsBachelors Degree in Chemistry.Previous laboratory experience in regulate

To provide technical expertise for the management of Environmental Health & Safety programs of the site. perform EH&S duties for program design development and implementation.Functions:Ensure compliance with EH&S federal state and local regulations. Evaluate existing and new regulatio

To provide technical expertise for the management of Environmental Health & Safety programs of the site. perform EH&S duties for program design development and implementation.Functions:Ensure compliance with EH&S federal state and local regulations. Evaluate existing and new regulatio

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