🛠 Tech Stack

💼 About This Role

You'll join Adverum Biotechnologies, a subsidiary of Eli Lilly, to manage document control and quality systems. You'll ensure MasterControl EQMS runs smoothly and support inspection readiness. This hybrid role in Redwood City offers a chance to impact gene therapy development.

🎯 What You'll Do

• Administer MasterControl EQMS and manage document lifecycles.
• Support version upgrades, configuration, and continuous improvement.
• Train users on MasterControl and resolve system issues.
• Prepare quality metrics and manage document control room.

📋 Requirements

• Bachelor's degree in Life Science or related field.
• 7+ years experience with electronic document management systems.
• 5 years Document Control, Training, or Quality System experience.
• Proficient in MS Office and Adobe Acrobat; knowledge of GMP regulations.

✨ Nice to Have

• Experience with implementation/maintenance of electronic document management systems.
• Curriculum design and training experience.

🎁 Benefits & Perks

• 📄 Contract role with competitive hourly rate.

📨 Hiring Process

Estimated timeline: 2-3 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical interview· 1 hour