Senior Validation Engineer – Pharmaceutical Systems

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

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.