Contract, CMC Project Manager (Biologics)

Stratacuity: Proven Scientific Placement; Cambridge (MA); On-site; USD 120,000 - 170,000; Full time

Job summary

Stratacuity: Proven Scientific Placement seeks a CMC Project Manager in Cambridge, MA to drive integrated development plans for biologics, including mAbs, fusion proteins, and bispecifics.

The role partners with CMC leads and cross-functional teams to manage timelines, identify risks, and ensure milestones are met, with external CDMO coordination and regulatory planning support. On-site in Cambridge four days a week.

Qualifications

• BS/MS in a scientific discipline.
• 5+ years of biopharmaceutical industry experience.
• Experience supporting CMC programs for biologics.
• Strong project management and cross-functional leadership skills.
• Experience working with CDMOs.
• Proficiency with Smartsheet, Office Timeline, or comparable platforms.

Responsibilities

• Partner with CMC leads and cross-functional teams to drive integrated development plans.
• Manage timelines, identify risks, and ensure alignment with key program milestones.
• Coordinate activities with external CDMO partners and support regulatory submission planning.
• Work on-site with Cambridge teams four days per week.

Skills

Project management

Cross-functional leadership

CDMO collaboration

Smartsheet

Office Timeline

Education

BS/MS in a scientific discipline

Tools

Smartsheet

Office Timeline

Job description

Our Cambridge based biotechnology company is seeking a CMC Project Manager to support the development of a growing portfolio of biologics, including monoclonal antibodies, fusion proteins, and bispecific antibodies.

In this role, you'll partner with CMC Technical Leads and cross-functional teams to drive integrated development plans, manage timelines, identify risks, and ensure alignment with key program milestones. You'll also coordinate activities with external CDMO partners and support regulatory submission planning. This position is on-site in Cambridge, MA 4 days per week.

Qualifications:

• BS/MS in a scientific discipline
• 5+ years of biopharmaceutical industry experience
• Experience supporting CMC programs for biologics
• Strong project management and cross-functional leadership skills
• Experience working with CDMOs
• Proficiency with tools such as Smartsheet, Office Timeline, or comparable platforms

Ideal candidates are highly organized, collaborative, proactive, and thrive in fast-paced biotech environments.