On Site Jobs
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Quality Engineer
Role: Quality EngineerSalary: $115,000 - $135,000Location: Minneapolis, MN A venture-backed, clinical-stage medical device innovator is advancing a minimally invasive, catheter-delivered Class III implantable system for structural heart disease. You'll join a small, high-ownership team at an exciting inflection point-helping build and execute valid...
Omaha Cardiology Account Manager
Role: Cardiology Account ManagerCompany: Mid-size biopharma companyTerritory: Omaha and Lincoln, Nebraska; Sioux Falls and Rapid City, South Dakota This role sits at the intersection of cardiology, heart failure, and hospital-based care and is a great fit for someone who enjoys running a territory independently and building strong HCP relationships...
Key Account Manager Atlanta/Nashville
Role: Key Account Manager Company: Mid-size biopharma company Territory: Atlanta, GA, Nashville, TN, and Birmingham, ALThis is a high-impact, field-based Key Account Manager role focused on driving access and adoption within complex health systems. It's a great fit for someone who enjoys working across institutional accounts, partnering cross-funct...
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Key Account Manager Carolinas
Role: Key Account Manager Company: Mid-size biopharma company Territory: CarolinasThis is a high-impact, field-based Key Account Manager role focused on driving access and adoption within complex health systems. It's a great fit for someone who enjoys working across institutional accounts, partnering cross-functionally, and building strong relation...
Sr Process Development Engineer
Senior Process Development Engineer Join a high-impact team advancing next-generation, minimally invasive therapies in the structural heart space. This is a rare opportunity to work hands-on with cutting-edge Class III devices that are pushing the boundaries of what's possible in cardiovascular treatment. What you'll do:Develop and optimize process...
Regulatory Affairs Lead
Regulatory Affairs LeadPosition Summary The Regulatory Affairs Lead will provide strategic and operational regulatory support across the product lifecycle for Class III medical devices. This role will partner cross‑functionally to help ensure regulatory alignment, support global submissions, and maintain compliance with applicable regulations.Key R...
