Senior Project Manager, Gene Editing

Danaher Corporation

. Serve as the primary client contact for gene editing and gRNA manufacturing programs .

Posted 10/16/2026full-timeCoralville • Iowa • United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in project management within the biotechnology and pharmaceutical sectors, with a strong focus on client engagement, risk management, and GMP product manufacturing processes. Proven ability to lead complex programs from initiation through to successful closure while maintaining high standards of quality and operational efficiency.

Highest-signal resume keywords

Project ManagementClient-Facing ExperienceGMP Product ManufacturingBiotechnology Industry ExperienceRisk Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project PlanningRisk Register ManagementAction Tracker DevelopmentStatus ReportingManufacturing Process KnowledgeQuality AssuranceProduct DevelopmentRegulatory ComplianceClient CommunicationProgram Leadership

Soft Skills

Team LeadershipClient Relationship ManagementProblem SolvingEffective CommunicationExpectation Management

Industry Keywords

BiotechnologyPharmaceuticalCDMOGMPBiological SciencesManufacturingQuality ControlProject GovernanceRisk AssessmentOperational Requirements

About the role

Key responsibilities & impact

Serve as the primary client contact for gene editing and gRNA manufacturing programs
Lead project team meetings and governance forums to align scope, timelines, risks, and deliverables
Develop and maintain project plans, status reports, risk registers, action trackers, and client and internal communications
Manage client expectations while balancing business, quality, and operational requirements
Identify, manage, and escalate critical risks and issues
Drive timely resolution across client programs and site-specific process and capability-building projects
Lead complex client programs from project initiation through manufacturing, release, and project closure

Requirements

What you’ll need

Bachelor’s degree in Biological Sciences or related field
8+ years of experience in the biotechnology, pharmaceutical, or CDMO industry, including significant project management experience and a technical background in product development, manufacturing, quality, or related scientific disciplines
Experience managing client-facing projects
Experience in a regulated biotechnology or pharmaceutical field or CDMO experience preferred
Understanding of GMP product manufacturing from initiation through release capabilities
Up to 15% travel may be required

Benefits

Comp & perks

Paid time off
Medical insurance
Dental insurance
Vision insurance
401(k)
Bonus/incentive pay eligibility
Comprehensive benefit programs
Reasonable accommodations for applicants and employees with disabilities