Validation Engineering Tech

About Us:BW Design Group is a fully integrated architecture, engineering, construction, system integration, and consulting firm committed to helping our clients realize their most critical goals from Strategy to Commercialization. As the only firm born from a manufacturing technology company to become an independent and fully integrated firm, we combine deep domain expertise in the manufacturing environment with an approach that is built to serve the dynamic needs of our clients. Rooted in our distinct culture of Truly Human Leadership, we cultivate the leaders who will define tomorrow and partner with our clients in the food & beverage, life sciences, industrial, and advanced technology industries to build the future of manufacturing and technology.Barry-Wehmiller is a diversified global supplier of engineering consulting and manufacturing technology for the packaging, corrugating, sheeting and paper-converting industries. Validation Engineer WhoYou’llWork WithYou will join one of our 45 offices in the US, bepart of a committed team ofover1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. When you join Design Group as aValidation Engineer II,you are joining a team that will challenge you andposition you for growth. You willjoin ourRegulatory Compliance Practiceandpartner with seasoned leaders, technicalspecialists, and subject matter expertsto deliver the highest quality solutions to our clients with consistency and accuracy.Together, you will help our clients make critical changes to improve their performance and realize their most important goals.Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment. This person will travel to top clients across the country toassistin the design of manufacturing processes, help manage projects, develop facilities, andimpactthe world by conducting themselves with integrity in pursuit of individual and enterprise goals. FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the pharmaceutical industryAssistin the development and execution of QMS procedures,ICH Q1 (Stability Protocols / Reports), CFR 21 Part 211, CFR 21 Part 820, ICH Q8, ICH Q9, and ICH Q10Work with teams to perform investigations and troubleshoot issues related to validationPrepare written validation reportsMake an impact day-to-day with your skills andexpertise, strengthening that relationship with our clients and teamWhatYou’llBringCandidates need topossessgood communicationand interpersonal skills, flexibility with tasks and the ability to interact with all levels of management, clients, and vendorsMinimum of 3 yearsproject experience with validation of automation, packaging,utilitiesand/or facilities Minimum of 3 yearsproject experience in the pharmaceutical or medical device environments Authoring CAPA's, deviations, SOP's is a plusStrong technical writing and oral communications Strong computer skills (Microsoft Office, Microsoft Project, & AutoCAD)Willing and able to travel as necessary for project requirements to include but notbe limitedto project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.You willbe surrounded by exceptional talentwho will supportyour development as both a world-class engineer andahighly effective leader.Company:Design GroupSummaryLocation: East Brunswick, NJType: Full time