Validation Engineer

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. By blending people-centric leadership with disciplined operational strategies and purpose-driven growth, Barry-Wehmiller has become a $3 billion organization with nearly 12,000 team members united by a common belief: to use the power of business to build a better world. Job Description: Validation Engineer Who   You’ll   Work With   You 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 make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class   professional consultant   and   surrounded by   leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.   When you join Design Group as a   Validation Engineer II,   you are joining a team that will challenge you and   position you for growth . In this role, you will work with   a team of   industry experts to help   the world’s leading companies   solve their most difficult problems. You will   join our   Regulatory Compliance Practice   and   partner with seasoned leaders, technical   specialists , and subject matter expert s   to deliver the highest quality solutions to our clients with consistency and accuracy.   What   You’ll   Do   You'll   work individually and in teams to   support capital projects   and implement solutions   for our   client s .   Together, you will help our clients make critical changes to improve their performance and realize their most important goals.   R esponsible 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 to   assist   in the design of manufacturing processes, help manage projects, develop facilities, and   impact   the world by conducting themselves with integrity in pursuit of individual and enterprise goals. This role will challenge you to be a passionate and successful business family   member all   while expanding your technical abilities.   FAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the pharmaceutical industry   Assist   in 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 Q10   Work with teams to perform investigations and troubleshoot issues related to validation   Prepare written validation reports   Make an impact day-to-day with your skills and   expertise , strengthening that relationship with our clients and team   What   You’ll   Bring   Candidates need to   possess   good communication   and interpersonal skills, flexibility with tasks and the ability to interact with all levels of management, clients, and vendors   Minimum of 3 years   project experience with validation of automation, packaging,   utilities   and/or facilities Minimum of 3 years   project experience in the pharmaceutical or medical device environments Authoring CAPA's, deviations, SOP's is a plus Strong 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 not   be limited   to project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc.   B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.   Our culture and commitment to our people is what sets us apart.   We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our   model and entrepreneurial mindset   offer a rewarding, challenging, and   highly   flexible path. As a   Validation Engineer II , you   will build a meaningful and fulfilling career   with the support of professional development   resources   and mentors hips   including   our   First Year Experience program, Individual Development Plans, and Career Path   resources   and tools.   You will   be surrounded by exceptional talent   who will support   your development as both a world-class engineer and   a   highly effective leader .   At Barry-Wehmiller we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job.  If your experience is close to what you see listed here, please still consider applying.  We know that our differences often can bring about innovation, excellence and meaningful work—therefore, people from all backgrounds are encouraged to apply to our positions.  Please let us know if you require reasonable accommodations during the interview process. ​ Barry-Wehmiller is an equal oppor