💼 About This Role

You'll be responsible for assisting the Validation manager in completing equipment and utilities qualifications for gene therapy production. Your core impact involves executing protocols, performing calibrations, and generating documentation in a cGMP environment. This temp role is onsite 5 days per week in Lexington, MA.

🎯 What You'll Do

• Execute site Re-Qualifications on equipment, utilities, and media fills.
• Generate and execute validation protocols and write final reports.
• Perform calibrations on thermocouples with data loggers in GMP/GXP.
• Collaborate with Manufacturing, Facilities, and Quality teams.

📋 Requirements

• AS degree or certificate in a science/technical field or trade school.
• 1+ years of relevant experience in a regulated (cGMP preferred) environment.
• Attention to detail and ability to multitask and prioritize.
• Experience with metrology/calibration principles.

✨ Nice to Have

• Experience with GE Kaye Validator and/or lives data acquisition systems.

🎁 Benefits & Perks

• 🏖️ Paid vacation days (amount based on tenure)
• 🏥 Choice of healthcare plans
• 💰 401(k) match up to 6%
• 📅 10 paid holidays + 2 floating + 1 volunteer day
• 🏢 Employee stock appreciation rights

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Technical Interview· 45 min
3. 3Offer· 1 week