Pharma Validation Engineer II - Regulatory & Quality Impact

Barry-Wehmiller Companies Inc.; East Brunswick Township (NJ); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Professional development resources

Mentorship opportunities

Flexible work environment

Job summary

A growing consulting firm in New Jersey is seeking a Validation Engineer II to develop and execute validation documents and assist in FDA compliance. The role demands strong communication and technical skills, along with at least 3 years of experience in validation processes within pharmaceutical or medical device sectors. Collaborate with teams to deliver high-quality solutions while travelling to client sites. Enjoy a culture of respect, integrity, and support for professional growth.

Qualifications

• Minimum of 3 years project experience with validation of automation and facilities.
• Project experience in the pharmaceutical or medical device environments required.
• Strong written and oral communication skills necessary.

Responsibilities

• Develop and execute validation and FDA compliance documents for pharmaceutical equipment.
• Conduct FAT, SAT, IQ, and OQ documentation for Automated Systems.
• Prepare written validation reports and assist in QMS procedures.

Skills

Communication skills

Interpersonal skills

Flexibility

Technical writing

Problem-solving

Project management

Tools

Microsoft Office

Microsoft Project

AutoCAD

Job description

A growing consulting firm in New Jersey is seeking a Validation Engineer II to develop and execute validation documents and assist in FDA compliance. The role demands strong communication and technical skills, along with at least 3 years of experience in validation processes within pharmaceutical or medical device sectors. Collaborate with teams to deliver high-quality solutions while travelling to client sites. Enjoy a culture of respect, integrity, and support for professional growth.