Validation Engineer

Validation Engineer II

Join BW Design Group to apply for the Validation Engineer role.

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 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.

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.

• Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment.
• Create FAT, SAT, IQ, and OQ documentation for automated systems in the pharmaceutical industry.
• Assist in the development and execution of QMS procedures, ICH Q1 (Stability Protocols/Reports), CFR 21 Part 211 and 820, ICH Q8, Q9, and 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 relationships with our clients and team.

• 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, biotechnology, or medical device environments is a plus.
• Experience in a gown‑room environment is a plus.
• Strong technical writing and oral communication abilities.
• Proficiency in Microsoft Office, Microsoft Project, and AutoCAD.
• Willingness and ability to travel as necessary for project requirements.
• B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree.

Associate

Full‑time

Quality Assurance

Barry‑Wehmiller is an equal‑opportunity employer. M/F/D/V. This organization uses E-Verify. 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. People from all backgrounds are encouraged to apply. Please let us know if you require reasonable accommodations during the interview process.

Applicants may be subject to pre‑employment screening, which may include drug screening, reference checks, employment verifications, background screening, and/or skills assessments.