Validation Engineer - Sterile Manufacturing

Validation Engineer - Sterile Manufacturing

Fairless Hills, PA

$85,000 - $100,000

Bonus Eligible (company performance based), 1st Shift, High-Impact GMP Role

Are you ready to join a sterile manufacturing site entering active production and play a direct role in qualifying the systems that make it run?

Do you want hands‑on ownership across equipment, process, and cleaning validation in a live GMP environment?

The site is transitioning into production, placing validation at the center of operations. Your work will directly support equipment qualification, aseptic processes, and overall manufacturing compliance as the business scales.

You will take ownership of equipment qualification activities, including IQ/OQ/PQ, playing a key role in bringing systems into a validated, production-ready state. You'll also contribute to process and cleaning validation efforts, working closely with Engineering, Quality, and Production teams to ensure systems are compliant and inspection-ready.

For someone with 2-5 years of GMP validation experience, this is a genuine opportunity to deepen sterile exposure, expand technical ownership, and position yourself for the next stage of growth within GMP manufacturing.

• Execute equipment, process, and cleaning validation within sterile operations
• Lead qualification activities and support validation documentation
• Contribute directly to production readiness and system qualification
• Maintain validation compliance within a GMP‑regulated site

• 2-5+ years of validation experience in pharmaceutical or biopharmaceutical manufacturing
• Exposure to sterile or aseptic environments
• Strong understanding of GMP documentation and compliance
• Motivated to take on broader validation responsibility

Reference Number: #BBBH
270163

We are an equal opportunities company and welcome applications from all suitable candidates.