Senior R&D Project Manager — Onsite CDMO Delivery

Evergen; Eden Prairie, Northern (MN, KY); Hybrid; USD 138,000 - 172,000; Part time

Job summary

Evergen seeks a Contractor – Senior R&D Project Manager for 100% onsite work in Eden Prairie, MN. You will lead CDMO project management from initiation to completion, including timelines, budgets, and stakeholder updates.

Drive cross-functional product development with global teams, assess risks, and coordinate transfer to manufacturing. 5+ years of PM/technical leadership in medical devices; PMP preferred; degree in a related field required.

Qualifications

• Bachelor’s degree in Material Science, Bioengineering, chemistry or engineering related field.
• 5+ years of project management/technical team leadership experience.
• PMP certification preferred.
• Ability to operate in a matrix organization with leadership, clients, and cross-border collaboration.

Responsibilities

• Champion and drive execution of CDMO Project Management activities including milestones, schedules, budgets, resources, status reports and communication.
• Prepare project plans, timelines, and budgets.
• Actively manage project timelines and budgets from initiation through completion, ensuring on-time delivery within budget.
• Ensure key stakeholders are informed of project status; manage resource allocation and risks.
• Track and communicate KPIs; collaborate with commercial team on proposals and quotations.
• Engage with global cross-functional product development teams; assist in design transfer and validation readiness.

Skills

Verbal & written communication

Microsoft Office Suite

Matrix organization

Time management

Medical device industry knowledge

Education

Bachelor’s degree in Material Science, Bioengineering, chemistry or engineering related field

Job description

Evergen seeks a Contractor – Senior R&D Project Manager for 100% onsite work in Eden Prairie, MN. You will lead CDMO project management from initiation to completion, including timelines, budgets, and stakeholder updates.

Drive cross-functional product development with global teams, assess risks, and coordinate transfer to manufacturing. 5+ years of PM/technical leadership in medical devices; PMP preferred; degree in a related field required.