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Validation Engineer

Job in Carmel, Hamilton County, Indiana, 46033, USA
Listing for: Caelum Research Corporation
Full Time position Listed on 2026-11-04
Job specializations:
Salary/Wage Range or Industry Benchmark: 95000 - 130000 USD Yearly USD 95000.00 130000.00 YEAR

Job Description & How to Apply Below

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

What You'll Do

You will 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. You will be 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 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 while expanding your technical abilities. Establish user requirement specification for critical equipment and systems. Assess risk across various aspects of systems' functions and focus efforts on critical quality aspects. Develop and execute validation and FDA compliance related documents/protocols for pharmaceutical equipment and processes including Process Equipment, Facility / Utilities, Cleaning / Process.

Work with teams to perform investigations and troubleshoot issues related to validation. Analyze qualification data and recommend corrective actions. Develop and perform impact assessments, trace matrices, system risk assessments, and other risk-based validation documentation deliverables. Prepare validation reports. Assist in project planning, scheduling, and coordination. Provide routine communication and status updates to BW Design Group for project leadership and the client.

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. Ability to work as an individual contributor as well as a team player on a large project team. Minimum of 7+ years project experience in the pharmaceutical or medical device environments. Strong technical writing and oral communications.

Strong computer skills (Microsoft Office, Microsoft Project, and AutoCAD). Willing and able to travel as necessary for project requirements to include but not limited to project installation and start-up activities, client meetings, company sponsored meetings, trainings, industry related seminars, forums, or conventions, etc. Understanding of ICH Q7 through 11, 21 CFR Parts 210, 211, 11, ISPE Baseline Guides, GAMP5, and ASTME
2500. B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.

Our Culture

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, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First-Year Experience program, Individual…

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