QRC Group, LLC

We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.Requirements3 to 5 years of experience in a GMP environment.Experience in the pharmaceutical industry.Knowledge of and experience with aseptic and regulated

We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.Requirements3 to 5 years of experience in a GMP environment.Experience in the pharmaceutical industry.Knowledge of and experience with aseptic and regulated

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 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 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