Validation Engineer

If you're the kind of Validation Engineer who actually likes owning the work - not just checking boxes - this is the type of role worth looking at. A growing life sciences engineering and compliance firm in the Princeton area is expanding its validation team and looking for engineers with real GMP validation experience across equipment, systems, and regulated processes. This team supports pharmaceutical, biotech, laboratory, and manufacturing environments where the work is highly visible, technically challenging, and genuinely important. You'll be involved in:

• Writing and executing

IQ/OQ/PQ

protocols

• Equipment and process qualification
• GMP/FDA regulated projects
• Cross-functional work with Quality, Engineering, and Operations
• Driving validation efforts from planning through execution This is a strong fit for someone coming from:
• Pharma or biotech manufacturing
• CQV/validation consulting
• Medical device or regulated environments
• GMP labs, pilot plants, or production facilities Why people tend to like environments like this:
• Diverse projects instead of the same equipment every day
• Strong technical exposure and career growth
• High-impact work in regulated industries
• Smaller, more agile team environment where engineers have real ownership
• Stable pipeline of life sciences projects in the NJ market

Seeking :

• 5+ years of validation experience
• Experience authoring and executing

IQ/OQ/PQ

• Strong GMP/FDA background
• Engineers comfortable leading validation efforts, not just supporting them Salary range: $100K-$125K depending on experience.

Pay:

$100,000.00 - $125,000.00 per year

Benefits:

401(k) Dental insurance Employee assistance program Health insurance Paid time off Professional development assistance Retirement plan Vision insurance

Work Location:

In person