Validation Engineer III

Barry-Wehmiller•Philadelphia, PA

1d•Hybrid

About The Position

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. When you join Design Group as a Validation Engineer III, 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.

Requirements

Minimum 5 years of demonstrated experience with commissioning, qualification, and validation (CQV) of pharmaceutical, biotech, or medical device processes, systems, and equipment
Experience with GMP Lifecycle Documentation development and execution experience (ex. - FAT, SAT, IQ, OQ, PQ, Risk Assessments, URS) in the Life Science Industry
Candidates need to possess excellent communication and interpersonal skills and have the ability to interact with all levels of management, clients, and vendors.
Strong computer skills are also required
Willingness and ability 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, training sessions, industry related seminars, forums, or conventions, etc.
Bachelor's degree in electrical engineering, Mechanical Engineering, Chemical Engineering, or equivalent technical degree.

Nice To Haves

CQV experience in the areas of automation, packaging, cleaning, computer systems, utilities and/or facilities is desired
Excellent organizational / leadership skills including the ability to simultaneously organize, and successfully execute multiple project responsibilities

Responsibilities

Responsible for preparing and executing commissioning and qualification documents for a variety of pharmaceutical/biotech/medical device utilities, facilities, and process equipment, with a focus on industry best practices, and with a consultant mindset and quality approach
Provide excellent communication, both written and verbal, to express information, project status, and technical questions or concerns as needed, to your project team leadership
Make an impact day-to-day with your skills and expertise, strengthening that relationships with our clients and teams