CSV Validation Specialists / Engineers
Support computerized systems, equipment, utilities, process, and validation activities within regulated life-science environments.
N&CS brings together technical, quality, validation, manufacturing and regulatory expertise. We are interested in professionals who can contribute practical solutions inside regulated environments.
Explore the areas of expertise N&CS needs across consulting, validation, quality, manufacturing and compliance.
Support computerized systems, equipment, utilities, process, and validation activities within regulated life-science environments.
Support investigations, root-cause analysis, CAPA development, effectiveness checks, quality-system remediation, and regulatory compliance initiatives.
Support manufacturing operations, process improvement, quality systems, investigations, equipment, and regulated production environments.
Support GMP, quality-system, regulatory compliance, remediation, inspection readiness, and GxP initiatives.
Support supplier qualification, quality audits, supplier performance, corrective actions, and quality-system requirements.
Support manufacturing processes, equipment, capacity, process improvement, troubleshooting, and technical initiatives within regulated facilities.
If your profile fits an available opportunity, a human resources representative will contact you to schedule a formal interview.
We are continuously seeking professionals with experience in pharmaceutical and medical-device quality, validation, manufacturing, engineering and regulatory environments.
Requirements typically include a relevant Bachelor degree, at least two years of industry experience, strong cGxP knowledge, documentation skills, the ability to manage multiple project tasks, and strong interpersonal and communication skills.
Project duration: varies from three months to one year.