QRC Group, LLC

We are seeking a Quality Associate to support and maintain quality systems ensuring compliance with GMP regulations industry standards and company policies within a regulated manufacturing environment. The successful candidate will be responsible for reviewing and managing quality doc

We are seeking a Quality Associate to support and maintain quality systems ensuring compliance with GMP regulations industry standards and company policies within a regulated manufacturing environment. The successful candidate will be responsible for reviewing and managing quality doc

We are seeking a Process Development Sr. Scientist to support scientific and technical activities within a regulated manufacturing environment. The ideal candidate will possess a strong scientific background experience with validation activities technical documentation and the ability

We are seeking a Process Development Sr. Scientist to support scientific and technical activities within a regulated manufacturing environment. The ideal candidate will possess a strong scientific background experience with validation activities technical documentation and the ability

We are seeking a Senior Process Development Scientist to support sterile drug product manufacturing operations within the pharmaceutical or biotechnology industry. The ideal candidate will have strong expertise in aseptic processing process characterization process validation technolo

We are seeking a Senior Process Development Scientist to support sterile drug product manufacturing operations within the pharmaceutical or biotechnology industry. The ideal candidate will have strong expertise in aseptic processing process characterization process validation technolo

To perform investigations for pharma-biotech industry supporting the complaints system. Investigations management including root cause analysis.Lead and manage investigations performing data analysis and trending of information to detect signals proactively and take appropriate action

To perform investigations for pharma-biotech industry supporting the complaints system. Investigations management including root cause analysis.Lead and manage investigations performing data analysis and trending of information to detect signals proactively and take appropriate action

QRC Group is seeking an experienced Quality Assurance Engineer to provide oversight and quality leadership for a major Grade D Manufacturing Environment project at a sterile combination drug/device manufacturing facility.This individual will serve as the Quality Assurance Engineer for

QRC Group is seeking an experienced Quality Assurance Engineer to provide oversight and quality leadership for a major Grade D Manufacturing Environment project at a sterile combination drug/device manufacturing facility.This individual will serve as the Quality Assurance Engineer for

We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requireme

We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requireme

We are seeking a Process Development Principal Scientist to support all phases of inspection project managementfrom planning and implementation to monitoring completion and follow-upensuring alignment with goals timelines and quality standards.Responsibilities:Lead PD related Project

We are seeking a Process Development Principal Scientist to support all phases of inspection project managementfrom planning and implementation to monitoring completion and follow-upensuring alignment with goals timelines and quality standards.Responsibilities:Lead PD related Project

We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requireme

We are seeking a Validation Specialist to support validation activities within the Molding area. The selected candidate will assist in the execution documentation and completion of validation projects while ensuring compliance with quality standards and applicable regulatory requireme

We are seeking a Process Development Principal Scientist to support all phases of inspection project managementfrom planning and implementation to monitoring completion and follow-upensuring alignment with goals timelines and quality standards.Responsibilities:Lead PD related Project

We are seeking a Process Development Principal Scientist to support all phases of inspection project managementfrom planning and implementation to monitoring completion and follow-upensuring alignment with goals timelines and quality standards.Responsibilities:Lead PD related Project

We are looking for motivated and detail-oriented Manufacturing Operators with a background in science or engineering who are looking to build experience in a regulated manufacturing environment (pharmaceutical/medical device).Key ResponsibilitiesOperate and monitor manufacturing equip

We are looking for motivated and detail-oriented Manufacturing Operators with a background in science or engineering who are looking to build experience in a regulated manufacturing environment (pharmaceutical/medical device).Key ResponsibilitiesOperate and monitor manufacturing equip

The CAPA / Complaints Technical Writer is responsible for authoring reviewing and maintaining high-quality documentation associated with Corrective and Preventive Actions (CAPA) customer complaints investigations non conformances and Quality Management System (QMS) remediation activit

The CAPA / Complaints Technical Writer is responsible for authoring reviewing and maintaining high-quality documentation associated with Corrective and Preventive Actions (CAPA) customer complaints investigations non conformances and Quality Management System (QMS) remediation activit

The Laboratory Investigations Scientist is responsible for conducting documenting and supporting investigations related to deviations out-of-specification (OOS) results and non-conformances associated with the testing and manufacturing of parenteral (sterile injectable) products. This

The Laboratory Investigations Scientist is responsible for conducting documenting and supporting investigations related to deviations out-of-specification (OOS) results and non-conformances associated with the testing and manufacturing of parenteral (sterile injectable) products. This

We are seeking a skilled Instrumentation Technician to support production operations. This role is responsible for calibrating and maintaining a wide range of instrumentation PLC and equipment critical to ensuring manufacturing quality and compliance.Key Responsibilities:Calibrate ins

We are seeking a skilled Instrumentation Technician to support production operations. This role is responsible for calibrating and maintaining a wide range of instrumentation PLC and equipment critical to ensuring manufacturing quality and compliance.Key Responsibilities:Calibrate ins

We are seeking a Specialist Quality Complaints.The primary responsibilities include: Supporting the product complaint system through; leading and managing product complaint investigations performing data analysis and trending of complaint information to detect signals proactively and

We are seeking a Specialist Quality Complaints.The primary responsibilities include: Supporting the product complaint system through; leading and managing product complaint investigations performing data analysis and trending of complaint information to detect signals proactively and

The EHS Manager is responsible for developing implementing maintaining and continuously improving site Environmental Health and Safety programs in support of regulatory compliance operational excellence and a strong safety culture. This role requires expertise in hazardous waste and t

The EHS Manager is responsible for developing implementing maintaining and continuously improving site Environmental Health and Safety programs in support of regulatory compliance operational excellence and a strong safety culture. This role requires expertise in hazardous waste and t

We are seeking a Documentation Specialist for Digital Operations to support manufacturing documentation activities including processes supported by the Tulip platform. This role is responsible for developing reviewing and maintaining controlled documents that support compliance tracea

We are seeking a Documentation Specialist for Digital Operations to support manufacturing documentation activities including processes supported by the Tulip platform. This role is responsible for developing reviewing and maintaining controlled documents that support compliance tracea

QA Investigations Lead to oversee and drive the end-to-end investigation processes within a regulated environment. This role will ensure timely compliant and effective resolution of quality events while providing strong project management oversight.The selected candidate will be resp

QA Investigations Lead to oversee and drive the end-to-end investigation processes within a regulated environment. This role will ensure timely compliant and effective resolution of quality events while providing strong project management oversight.The selected candidate will be resp

The Process Engineer is responsible for ensuring the reliability compliance and performance of manufacturing processes equipment utilities and computerized systems within a pharmaceutical or biotechnological environment. This role requires strong expertise in process engineering compu

The Process Engineer is responsible for ensuring the reliability compliance and performance of manufacturing processes equipment utilities and computerized systems within a pharmaceutical or biotechnological environment. This role requires strong expertise in process engineering compu