Technical Project Manager II Client-facing RNA/ DNA Mfg., Method Development/ Validation - danaher

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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.

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The Technical Project Manager (TPM) II is responsible for managing the development elements of biomanufacturing projects in support of client programs and services.

This position reports to the Manager of Technical Project Management and is part of the Project Management team located in Fargo, ND, and will be an on-site role.

In this role, you will be expected to:

• Oversee complex biomanufacturing projects utilizing department standards and tools.
• Work collaboratively with the Project Managers, internal stakeholders, Program Managers, and clients while maintaining the project timeline data, communicating project status updates, managing project changes, ensuring timely achievement of key milestones, and tracking and driving the completion of action items and project deliverables.
• Proactively identify potential obstacles and work alongside cross-functional teams to develop and execute effective solutions.
• Resolve conflicts and remove roadblocks with internal and external stakeholders in a constructive manner to preserve and strengthen professional relationships.

The essential requirements of the job include:

• Bachelor’s degree or higher in Biological Sciences, Chemistry, or a related discipline.
• Prefer 3+ years of experience in method development, method validation, quality control, biomanufacturing validation, process development, or technology transfer, ideally pertaining to nucleic acids.
• Proven experience successfully leading relevant departments and/or managing complex projects with both waterfall and agile methodologies.