18 results for Validation Engineer Jobs in Raleigh, NC, US

Develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. Responsible for protocol writing, execution, and summary report development. Plans and coordinates work, directing small teams in document development and execution.

Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec's mission is to provide a wide spectrum of services that help its clients meet their capital ...

Responsible for leading or contributing to hardware and software design of process automation control systems projects, including defining architecture requirements, developing test protocols, and creating SAT/FAT documentation. Involves reviewing documentation, maintaining project documentation, an...

Are you an automation expert with a passion for solving complex challenges? Bring your DeltaV expertise to a consultative role where you will design, implement and maintain cutting-edge solutions!We are seeking a mid-level Automation Engineer with 2-5 years of experience to support process automatio...

Welcome to the forefront of innovation in cutting edge patient treatments! We are thrilled to present an incredible opportunity to join our high performing organization. As a leader within the life science industry, we are constantly pushing the boundaries of what is possible and redefining the stan...

We are seeking a proactive and detail-oriented CQV Engineer to support our client’s pharmaceutical and life sciences projects in the Raleigh/Durham area. This individual will play a key role in commissioning, qualification, and validation (CQV) activities for equipment and systems. The ideal candida...

Piper Companies is actively seeking a Validation and Technical Support Engineer to join a global pharmaceutical organization producing innovative, injectable diabetes and obesity treatment. The successful candidate will provide validation and technical support through the preparation, execution, dat...

ResponsibilitiesConduct Computer System Validation (CSV) for pharmaceutical systems to ensure they comply with FDA regulations and industry standards (e.g., GAMP 5). Lead and execute Equipment Validation activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Perfo...