13 results for Validation Engineer Jobs in Severn, MD, US

ResponsibilitiesResponsible for preparing, executing commissioning and qualification documents for a variety of utilities, facility, and process equipment.Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.Make an impact day-to-day...

Wunderlich-Malec Engineering (WM) is a 100% employee-owned ESOP and one of the largest and most well-established engineering companies in the United States. When you join WM you become part of a company that is:100% employee-owned with 40+ years of industry historyENR (Engineering News Record) Top 5...

Responsible for participating in validation projects related to manufacturing equipment and critical computer systems. Duties include authoring and reviewing validation protocols and deliverables, coordinating multiple projects, ensuring compliance with data integrity and regulatory standards, and c...

Define, analyze, and validate system and subsystem requirements for digital telecommunications payloads. Develop and execute verification plans, lead or support system-level payload test campaigns, and interface with hardware and software teams. Participate in technical reviews and support anomaly i...

Job Title: Payload System Verification and Validation EngineerJob DescriptionAs a Payload System Verification and Validation Engineer, you will define, analyze, and validate system and subsystem requirements for digital telecommunications payloads. You will develop and execute verification plans, in...

Define, analyze, and validate system and subsystem requirements for digital telecommunications payloads. Develop and execute verification plans, lead or support test campaigns, and interface with hardware and software teams. Participate in technical reviews and support anomaly investigation. Contrib...

Position DescriptionThe Computer Systems Validation (CSV) Engineer is responsible for writing GxP computer validation and 21 CFR Part 11 related documentation such as assessments, plans, URS, FRS, RTM, and summary reports. Where required, they will be expected to develop and execute protocols and te...

Who You’ll Work WithYou will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to ma...

Position Summary:Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, ...

Responsible for writing GxP computer validation documentation, developing and executing protocols and test scripts, and ensuring compliance with 21 CFR Part 11. Works with various major systems in biotech and pharma, and may require travel domestically and internationally.