Validation Engineer III
On-site · Philadelphia, Pennsylvania, United States
Job Summary
Validation Engineer III responsible for preparing and executing commissioning and qualification documents for pharmaceutical/biotech/medical device utilities, facilities, and process equipment, with a focus on industry best practices and a consultant mindset. Collaborates with a team of industry experts to deliver high-quality solutions, communicates project status effectively, and contributes to the BW Design Group’s technical consulting strategy. Requires minimum 5 years CQV experience, GMP lifecycle documentation expertise (FAT, SAT, IQ, OQ, PQ, risk assessments, URS), and a relevant engineering degree. Willingness to travel to support project installation, start-up activities, client meetings, training sessions, and related events. The role emphasizes teamwork, client relationships, and professional development within a globally distributed engineering consulting environment.
Required Qualifications
- 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 (FAT, SAT, IQ, OQ, PQ, Risk Assessments, URS) in the Life Science Industry
- CQV experience in automation, packaging, cleaning, computer systems, utilities and/or facilities is desired
- Excellent organizational/leadership skills with ability to manage multiple project responsibilities
- Strong communication and interpersonal skills; ability to interact with all levels of management, clients, and vendors
- Willingness and ability to travel for project requirements
- Bachelor's degree in electrical, mechanical, chemical engineering, or equivalent technical degree
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