Program Management Sr. Manager

📋 Description

• Organize CMC/QA activities and deliverables; run weekly meetings.
• Interface with CDMOs to drive manufacturing per CMC timelines.
• Draft regulatory filing sections; coordinate cross-functional reviews.
• Coordinate document QC to ensure content accuracy.
• Contribute to long-range planning and budgeting; manage vendor contracts/POs.
• Communicate effectively with internal and external stakeholders.

🎯 Requirements

• M.S. or B.S. in chemistry or chemical engineering preferred
• 10+ years biotech/pharma project management experience
• Strong planning, tracking, multitasking, and prioritization
• Ability to work strategically with internal and external groups
• Excellent communication with internal and external stakeholders
• Up to 10% travel required

🎁 Benefits

• 100% employer-paid medical, dental, vision for you and dependents
• 401(k) with employer match
• Subsidized lunch and parking on in-office days
• Hybrid work model with in-office 2-3x per week
• Flexible PTO and company-paid holidays
• Career development via LinkedIn Learning, LifeLabs, BetterUp