Project Manager, Validation

Project Manager, ValidationYou 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.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 experts to deliver the highest quality solutions to our clients with consistency and accuracy.You'll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.Responsible for preparing, executing commissioning and qualification documents for a variety of utility, facility, and process equipment.Lead and manage a diverse portfolio of validation projects simultaneously (equipment qualification, process validation, cleaning validation, system digitization, etc.)Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.Serve as the primary on-site point of contact and local engineering leader for major pharmaceutical manufacturing clientsBuild and maintain strong relationships with client stakeholders across operations, quality, regulatory, and executive levelsMake an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and teamWhat You'll BringMinimum 10+ years of demonstrated experience with validation of pharmaceutical or medical device processes and equipmentFAT, SAT, IQ and OQ documentation development and execution on Automated Systems in the Pharmaceutical IndustryValidation experience in the areas of automation, packaging, cleaning, Computer systems, utilities and/or facilities is desiredExcellent leadership skills including the ability to simultaneously organize, and successfully execute multiple project responsibilitiesCandidates need to possess good communication and interpersonal skills and the ability to interact with all levels of management, clients, and vendors.Strong computer skills are also requiredWilling 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.Bachelor's degree in Chemical Engineering, Biomedical Engineering, Electrical Engineering, Mechanical Engineering or equivalent 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 Sr. Validation Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships 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.Barry-Wehmiller is an equal opportunity employer. M/F/D/V This organization uses E-Verify.Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.