We are seeking an experienced and hands-on Director of Research & Development to lead product innovation and development at a growing medical device contract development and manufacturing organization (CDMO). This leader will oversee R&D initiatives, driving catheter design and development programs while mentoring and managing a cross-functional team. The role requires a balance of strategic vision and day-to-day technical leadership in a regulated, cleanroom environment.
Job Location: Minneapolis / St. Paul
Kidney Scientist
About the Company:
A pioneering biotechnology company advancing regenerative therapies to address critical gaps in transplant medicine. The organization is developing innovative, tissue-engineered solutions through decellularization and recellularization techniques, with the goal of restoring function in patients with end-stage organ disease. The team brings together cross-disciplinary expertise and a mission-driven focus to push the boundaries of organ and tissue science.
Position Overview:
The Kidney Scientist will play a central role in the advancement of bioengineered kidney development efforts. This individual will lead or support experimental design, execution, and analysis related to tissue engineering, cell biology, and kidney function assays. The ideal candidate brings hands-on experience with kidney physiology, nephrology research, and/or tissue-engineered constructs, and is motivated to help bring functional organs closer to clinical application.
Associate Director of Regulatory Affairs
About the Company:
A growing life sciences company focused on breakthrough advancements in regenerative therapies. The organization is pioneering technologies aimed at addressing critical unmet needs in transplant and cell-based treatment options. Backed by a mission-driven team, the company is committed to reshaping the future of advanced therapies through science-driven innovation.
Position Overview:
The Associate Director of Regulatory Affairs will lead regulatory strategy and operations for both preclinical and clinical-stage programs. This individual will be responsible for ensuring compliance with all relevant FDA regulations, including but not limited to CFR 1271 and guidance provided by CBER. The ideal candidate has hands-on experience in regulatory submissions, strategic interactions with the FDA, and thrives in a cross-functional, fast-paced environment.
