Senior Manager, Biologics CMC Project Management

Scorpion Therapeutics; Wilmington (DE); Hybrid; USD 120,000 - 160,000; Full time

Job summary

Incyte is seeking a Senior Manager, Biologics CMC Project Management within the Tech Ops Global Biologics Development group. The role leads cross-functional coordination for biologics development programs across all stages.

You will develop integrated project plans, track dependencies, and identify risks while supporting resource and budget management. Interaction with CMOs/CROs and contributing to lifecycle management are key aspects of the role.

Qualifications

• 4–6+ years supporting biologics product development in pharma/biotech, with experience in CMC project activities and understanding of regulatory requirements.
• Strong project management, facilitation, communication, and influence skills; PMP preferred.

Responsibilities

• Develop integrated project plans and track dependencies.
• Identify and elevate risks; manage resource and budget support.
• Prepare governance materials and coordinate with external partners like CMOs and CROs.
• Contribute to lifecycle management and submission timelines, ensuring aligned execution and visibility.

Skills

Project management

Facilitation

Communication

Influence

PMP

Education

BS/MS/PhD in Biological Sciences or related

Job description

Role

Senior Manager, Biologics CMC Project Management within Incyte's Tech Ops Global Biologics Development group, leading cross-functional project coordination for biologics development programs across all stages.

Responsibilities

• develop integrated project plans
• track dependencies
• identify and elevate risks
• support resource and budget management
• prepare governance materials
• coordinate with external partners like CMOs and CROs.
• Contribute to lifecycle management and submission timelines, ensuring aligned execution and visibility.

Qualifications

4-6+ years supporting biologics product development in pharma/biotech, with experience in CMC project activities and understanding of regulatory requirements.

Education

BS/MS/PhD in Biological Sciences or related.

Skills

strong project management, facilitation, communication, and influence skills; PMP preferred.

HighValue

biologics (monoclonal antibodies), CMC development, cross-functional coordination, mid-to-late stage development, regulatory submissions, external vendor management.

WorkSetup

hybrid, with occasional international travel.