Pharma Validation Engineer II – Travel & Impact

Barry-Wehmiller Companies Inc.; Clearwater (FL); On-site; USD 90,000 - 120,000; Full time

Job summary

Barry-Wehmiller Design Group is seeking a Validation Engineer II to join our Regulatory Compliance Practice. You will work with a team of industry experts to develop validation and FDA compliance documentation for pharmaceutical equipment and support capital projects across the country.

You will travel to client sites to assist in design, facility development, and startup activities, while delivering high-quality validation reports and maintaining strong written and oral communication with

Qualifications

• 3+ years project experience with validation of automation, packaging, utilities and/or facilities is desired.
• Pharmaceutical or medical device environments experience is a plus.
• Strong technical writing and oral communications.

Responsibilities

• Support capital projects and implement solutions for our clients.
• Develop and execute validation and FDA compliance documents/protocols for pharmaceutical equipment.
• Travel to top clients across the country to assist in design, manufacturing facilities and startup activities.
• Prepare written validation reports.
• FAT, SAT, IQ and OQ documentation development and execution on automated systems in the pharmaceutical industry.

Skills

Communication skills

Interpersonal skills

Willingness to travel

Education

B.S. in Bioengineering

Tools

Microsoft Office

Microsoft Project

AutoCAD

Job description

Barry-Wehmiller Design Group is seeking a Validation Engineer II to join our Regulatory Compliance Practice. You will work with a team of industry experts to develop validation and FDA compliance documentation for pharmaceutical equipment and support capital projects across the country.

You will travel to client sites to assist in design, facility development, and startup activities, while delivering high-quality validation reports and maintaining strong written and oral communication with