🛠 Tech Stack

💼 About This Role

You'll manage end-to-end QC project timelines for a clinical-stage gene therapy company, coordinating method validation and PPQ readiness. You'll partner with cross-functional teams to align deliverables with regulatory milestones. This is a contract role at a subsidiary of Eli Lilly.

🎯 What You'll Do

• Manage QC project timelines for method validation and PPQ readiness.
• Coordinate cross-functional QC and QA activities to meet milestones.
• Identify risks, dependencies, and delays; escalate as needed.
• Facilitate team meetings, document minutes, and track action items.

📋 Requirements

• Bachelor's degree in a scientific discipline (Biology, Chemistry, etc.).
• 5+ years of experience including QC lab or project coordination in pharma/biotech.
• Strong understanding of QC lab workflows and GMP environments.
• Proficiency with Microsoft Project or similar timeline tracking tools.

✨ Nice to Have

• Prior hands-on laboratory experience.
• Experience working with external vendors.
• Ability to travel occasionally.

🎁 Benefits & Perks

• 💵 Contract hourly rate $50-55/hr

🚩 Heads Up

• Contract role listed under 'QC Project Manager' but requires 5+ years experience with senior-level responsibilities.
• Salary range is hourly ($50-55/hr) yet listed as contract; unclear if benefits are included.