Sr. Project Manager, Gene Editing (Client-Facing)

Radiometer; Coralville (IA); On-site; USD 110,000 - 160,000; Full time

Benefits offered by this job

Bonus/incentive pay

Medical/dental/vision insurance

401(k)

Job summary

Aldevron, a Danaher operating company, is seeking a Senior Project Manager, Gene Editing in Coralville, IA. You will lead GMP gRNA manufacturing programs, serve as the primary client contact, and drive cross-functional execution from initiation to release and closure.

You’ll develop project plans, manage risks, and align scope with quality and operations while coordinating governance forums and client communications. Travel up to 15% may be required.

Qualifications

• Bachelor’s degree in Biological Sciences or related field, Masters or PhD preferred.
• Experience managing client-facing projects in biotechnology/pharma or CDMO.
• Understanding GMP product manufacturing from initiation through release capabilities.

Responsibilities

• Serve as the primary client contact for gene editing and gRNA manufacturing programs.
• Lead project team meetings and governance forums to ensure alignment on scope, timelines, risks, and deliverables.
• Develop and maintain project plans, status reports, risk registers, and client/internal communications.
• Manage client expectations while balancing business, quality, and operational requirements.
• Identify, manage, and escalate critical risks and issues, driving timely resolution.

Skills

Project management

Client management

Cross-functional leadership

Education

Bachelor’s degree in Biological Sciences

Masters or PhD preferred

Job description

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Aldevron, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking therapies. Our mission is to be the engine of innovation for genomic medicine pioneers. As a member of our team, you’ll help bring life-changing innovations to life—impacting millions around the world. We bring together deep scientific expertise, an unwavering commitment to quality, and a collaborative spirit to drive progress. Whether you're launching your career or bringing years of experience, we value the unique perspective you bring. Join us and become part of a mission-driven team advancing science and unlocking human potential—one discovery at a time. Learn about the Danaher Business System which makes everything possible.

The Senior Project Manager, Gene Editing is responsible for leading complex client programs focused on GMP guide RNA (gRNA) manufacturing and related gene editing products. This role serves as the primary point of contact for clients and is accountable for driving cross-functional execution from project initiation through manufacturing, release, and project closure. This position reports into the Project Management team, and is located in Coralville, IA and will be an on-site role.

In this role, you will have the opportunity to:

• Serve as the primary client contact for gene editing and gRNA manufacturing programs.
• Lead project team meetings and governance forums to ensure alignment on scope, timelines, risks, and deliverables.
• Develop and maintain project plans, status reports, risk registers, action trackers, and client and internal communications for client programs and site-specific process and capability-building projects.
• Manage client expectations while balancing business, quality, and operational requirements.
• Identify, manage, and escalated critical risks and issues, driving timely resolution across client programs and site-specific process and capability-building projects.

The essential requirements of the job include:

• Bachelor’s degree in Biological Sciences or related field, Masters or PhD preferred.
• Prefer 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
• Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role
• This role may include up to 15% travel.

Aldevron, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

For more information, visit www.danaher.com.

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