Validation Engineer III

Barry-Wehmiller Companies Inc.; Philadelphia, Northern (Philadelphia County, KY); Hybrid; USD 90,000 - 130,000; Full time

Job summary

BW Design Group is seeking a Validation Engineer III to support capital projects, validate pharmaceutical equipment, and ensure regulatory compliance. You will work with a team of industry experts to deliver high-quality validation documentation and develop robust validation strategies.

The role requires strong technical writing, ability to travel for project requirements, and collaboration across engineering, quality, and client teams.

Qualifications

• 7+ years of project experience with validation of automation, packaging, utilities and/or facilities.
• 3+ years of project experience in pharmaceutical or medical device environments is a plus.
• Strong technical writing and oral communications.
• Proficiency in MS Office, Project management, and CAD tools.

Responsibilities

• Develop and execute validation and FDA compliance related documents/protocols for pharmaceutical equipment.
• Travel to top clients across the country to assist in design of manufacturing processes and manage projects.
• FAT, SAT, IQ and OQ documentation development and execution on automated systems in the pharmaceutical industry.
• Assist in development and execution of QMS procedures and regulatory standards.
• Work with teams to perform investigations and troubleshoot issues related to validation.
• Prepare written validation reports.

Skills

Communication skills

Interpersonal skills

Technical writing

Microsoft Office

AutoCAD

Willing to travel

Team collaboration

Regulatory compliance

Education

B.S. in Bioengineering/Biomedical/Chemical Engineering or related technical degree

Tools

Microsoft Project

AutoCAD

MS Office

Job description

## Validation Engineer IIIApply: Philadelphia, PA: Full time: Posted Today: R021388**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 III **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 experts 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 clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals. + 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 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 7+ years project experience with validation of automation, packaging, utilities and/or facilities is desired + Minimum of 3 years project experience in the pharmaceutical or medical device environments 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 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. #LI-TH1* Additional Job Description Establishes validation standards, develops and executes validation protocols, reports on findings, and oversees resolution of compliance failures or deviation Develops and maintains validation-related documentation, which may include specifications, SOPs, work instructions, or batch or testing records Ensures processes, products, equipment, or systems comply with all applicable external regulations or standards May assist with new equipment purchases or upgrades to existing equipment