readiness team in a timely and professional manner. Requirements: Bachelor's degree in a scientific discipline such as life... sciences, pharmacy, bioscience; advanced degree preferred. 5+ years of experience in regulatory affairs within the...
Responsibilities: Develop and coordinate execution of protocols for equipment (IQ/OQ/PQ) and process validations, prepare final reports following the execution. Support evaluation and analysis of data, lead investigation and documentati...
Responsibilities: Previous experience in label design work, with preference in any of the following labeling design systems: Software, Bartender, enable. Experience working with document control systems, especially Windchill. Design e...
Responsibilities: Develop, execute, and review comprehensive validation protocols for autoclaves and sterilizers, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). * Conduct...
Responsibilities and Requirements: We are seeking an experienced Computer System Validation (CSV) Engineer to join our team for an onsite project in Texas. The role involves validating the Meridian Electronic Document Management System (...
Responsibilities: Participate in the execution of global studies for regulatory submissions, reimbursement, and product adoption, including clinical study documents (protocol, case report forms, etc.), study implementation and data manage...
Responsibilities: Must have Skills are Docker, DevOps, AZURE, PowerShell, YAML, Jenkins, Kubernetes Design, implement, and maintain scalable and robust CI/CD pipelines using Azure DevOps. Must have hands on writing the scripts using She...
Responsibilities: Responsibilities for this role include deploying physical devices, configuring, and maintaining them by using cloud services, and maintaining and troubleshooting the configuration throughout the device lifecycle. IoT de...