Validation Engineer III

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:Job SummaryThe Validation Engineer III will serve as a key member of the validation team, providing expert-level support to ensure facility equipment, utilities, processes, instrumentation, and computerized systems are qualified and maintained in a validated state in compliance with applicable regulatory requirements. This role functions as a Validation Subject Matter Expert (SME) responsible for leading validation activities, authoring protocols and reports, and providing technical guidance to cross-functional teams. The Validation Engineer III will coordinate and execute qualification activities while collaborating with internal stakeholders and external vendors to support ongoing operations and capital projects.Key ResponsibilitiesValidation Documentation & ExecutionAuthor, review, and approve validation protocols, reports, and associated documentation including acceptance criteria developmentEstablish, revise, and maintain validation master plans, procedures, and lifecycle documentation for qualification of equipment, systems, and processes in accordance with cGMP requirementsExecute and oversee IQ/OQ/PQ protocols for equipment, utilities, and systemsReview and complete documentation in accordance with cGMP, ALCOA+ principles, and data integrity requirementsProject & Program ManagementLead and manage validation-related project activities including scheduling, resource coordination, protocol execution, and report reviewManage external vendors and contractors performing qualification activitiesServe as a key member of project teams for design, procurement, installation, and commissioning of new equipment and facility expansion projectsDevelop and maintain validation project timelines and deliverablesCompliance & Change ControlReview proposed changes to validated systems and provide impact assessmentsIdentify validation requirements necessary to maintain systems in a validated state following change implementationManage periodic requalification activities to ensure equipment, utilities, and processes remain compliantSupport equipment and building monitoring systems compliance and updatesTechnical ExpertiseServe as Subject Matter Expert (SME) in one or more of the following disciplines:Process MappingQuality Management (Quality Risk Assessments; Change Controls; Deviations; CAPA; Documentation)Equipment qualification (autoclaves, controlled temperature units, filling equipment)Cleaning validation Aseptic process simulation (media fills)Computer system validation (CSV)Process validation Utility qualification (WFI, purified water, clean steam, HVAC)Environmental monitoring systemsProvide technical guidance and troubleshooting support for equipment and system failuresDeliver training on validation program elements to junior validation personnelQuality Systems SupportAuthor and support equipment and process-related deviation investigations and CAPA activitiesPerform and support risk assessments (FMEA, etc.) and data integrity assessmentsSupport internal audits and regulatory agency inspectionsEnsure all work is performed in accordance with SOPs, cGMPs, quality standards, and safety proceduresQualificationsEducationBachelor's degree in Engineering, Life Sciences, or related scientific discipline requiredMaster's degree (MS/MSc) preferredExperienceMinimum 5+ years of professional experience in validation, engineering, or operations within a regulated environmentMinimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device manufacturing environmentDemonstrated expertise as a Subject Matter Expert (SME) in one or more validation disciplinesExperience with GMP utilities (WFI, purified water, clean steam, compressed gases, HVAC) and manufacturing equipmentExperience supporting regulatory inspections (FDA, EMA, or equivalent) preferredCapital project experience including equipment design, selection, and commissioning preferredSkills & CompetenciesStrong technical writing skills with ability to author clear, compliant documentationSolid working knowledge of cGMP regulations, FDA guidance documents, and industry standards (ISPE, PDA, GAMP)Understanding of GDP requirements and ALCOA+ data integrity principlesExcellent communication and interpersonal skills with ability to interface across all organizational levelsStrong project management and organizational skillsAbility to work independently with minimal supervision while also functioning effectively in a team environmentSelf-motivated with demonstrated initiative and problem-solving abilitiesProficiency in Microsoft Office Suite; experience with electronic validation systems a plusWorking ConditionsOn-site presence required; may involve work in manufacturing, laboratory, and utility areasAbility to gown into cleanroom environments as requiredOccasional flexibility in schedule and travel may be needed to support project timelines or production schedules#LI-TH1At 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 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.Company:Design GroupSummaryLocation: Boston, MAType: Full time