💼 About This Role

You'll support commissioning and qualification of GMP equipment for life sciences clients. Your work ensures life-changing drugs reach patients through validated manufacturing systems. You'll receive structured mentorship from experienced engineers.

🎯 What You'll Do

• Execute IQ, OQ, and PQ protocols for GMP equipment.
• Assist in developing validation deliverables (URS, DQ, etc.).
• Document test results and communicate issues to the team.
• Support commissioning activities and troubleshoot equipment issues.

📋 Requirements

• Bachelor's degree in engineering or Life Sciences.
• 0-2 years of experience in regulated manufacturing.
• Interest in pharmaceutical or biotechnology manufacturing.
• Basic understanding of GMP concepts.

✨ Nice to Have

• Exposure to IQ, OQ, and PQ activities.
• Familiarity with manufacturing equipment or automated systems.

🎁 Benefits & Perks

• 🏥 Premium medical coverage
• 💰 401(k) with company match
• 📚 Tuition reimbursement
• 🎯 Performance incentives
• 🏢 Employee Stock Ownership Plan (ESOP)