QRC Group

We are seeking a Quality Systems Specialist who will support the execution and maintenance of the Quality Management System (QMS) Remediation Plan in compliance with ISO 13485 FDA 21 CFR Part 820 (QMSR) EU MDR 2017/745 applicable regulatory requirements and company procedures.The Qual

We are seeking a Quality Systems Specialist who will support the execution and maintenance of the Quality Management System (QMS) Remediation Plan in compliance with ISO 13485 FDA 21 CFR Part 820 (QMSR) EU MDR 2017/745 applicable regulatory requirements and company procedures.The Qual

We are seeking Sr Engineer with experience in Medical Devices or Pharma industry.Duties: 1. C&Q Strategy & PlanningDevelop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.Define system boundaries and identify direct/ind

We are seeking Sr Engineer with experience in Medical Devices or Pharma industry.Duties: 1. C&Q Strategy & PlanningDevelop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.Define system boundaries and identify direct/ind