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À propos de ce poste Sr. Project Manager, Gene Editing (Client-Facing) chez Danaher

Danaher · Sur site · Coralville, Iowa, United States


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 escalate 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.


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Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.


For more information, visit www.danaher.com.


Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.


The U.S. EEO posters are available here.


For candidates who are based outside of New York City or who are applying for roles outside of New York City, for more information about conditions of any job offer please click here.


We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [email protected].

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À propos de Danaher

Danaher is a leading global life sciences, biotechnology, and diagnostics innovator, helping to solve many of the world’s most important health challenges, ultimately improving quality of life for billions of people today, while setting the foundation for a healthier, more sustainable tomorrow. The Danaher ecosystem is made up of more than 15 businesses united by a shared commitment to innovate for tangible impact. Please read our Applicant Data Privacy Notice carefully here .

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