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Our client is an innovative cardiovascular medical device company developing minimally invasive therapies for patients with heart failure. As their clinical programs expand globally, they are adding a Senior/Principal Clinical Evidence Specialist to their Clinical team. This newly created, high-impact role will report directly to the Vice President of Clinical, who brings a strong biostatistics background. The role is

Our client is an innovative structural heart medical device company developing therapies that improve patients' lives. They are adding a Clinical Education & Training Specialist to support their growing Clinical team and play a key role in physician education, patient case preparation, and clinical training as they advance their pivotal clinical trial. If you enjoy transforming complex clinical information into

We've partnered with our start-up structural heart client as they are seeking a PhD-level Clinical Science Specialist / Manager to serve as a key scientific contributor across clinical, regulatory, and R&D. This role sits at the intersection of data, physicians, and product development—translating complex clinical evidence into clear insights, publications, and strategic direction. This is

Our client, a growing medical device company , is adding a Senior Design Assurance Engineer to play a key role in the development and commercialization of an innovative device. This is an opportunity to work on a complex Class III implantable device as the company advances toward significant regulatory and commercialization milestones, including PMA and CE Mark approval . The Senior Design

Due to an internal promotion , our small, growing medical device client is adding a Clinical Trial Coordinator to provide critical coordination and operational support across the Clinical Operations team. This is a highly collaborative, hands-on role that touches many aspects of clinical trial execution: from site documentation and clinical data to payments, device logistics, meetings, and training. For someone

Our smaller medical device client is adding a Clinical Specialist II to the team. This is a critical, field-facing role supporting multi-center clinical trials and early commercial activities. This position drives patient enrollment, supports complex cases, and ensures clinical studies are conducted in accordance with GCP, ISO 14155, and regulatory requirements. You will serve as a clinical expert

If you’ve owned adverse event processing in a clinical trial…this will feel very familiar. We’re partnering with a structural heart company in Minnesota on a Clinical Safety Specialist role supporting an investigational heart valve program. This is a fully on-site, execution-heavy role—not a strategy or oversight role. You’re in it day-to-day

We are partnering with an innovative medical device company to add a Sr. Clinical Trial Specialist to support the day-to-day operations of global clinical studies. This is an excellent opportunity for someone who enjoys working in a fast-paced, collaborative environment and wants to play a key role in bringing new medical technologies to market. Your role with

Our client is an innovative structural heart medical device company developing a first-in-class Transcatheter Mitral Valve Replacement (TMVR) technology designed to transform the treatment of mitral regurgitation. They are seeking an experienced Research & Development Engineer who can bridge the gap between clinical procedures and product design. This highly visible role will focus on gathering physician and procedural

Are you a highly motivated Clinical Research Associate looking to make a significant impact in a growing medical device company? Our start-up client is seeking a driven CRA 2 to join their Clinical Operations team and play a pivotal role in post-FDA-approval data collection for their innovative product. This is an exciting opportunity to contribute to a

Want to help build a next-generation structural heart company from the ground up? This is an opportunity to join an innovative medical device startup developing Class III implantable valve and catheter-based delivery technologies that are advancing the future of cardiovascular care. They are looking for a hands-on Quality Engineer who thrives in fast-paced, collaborative environments and

Our client, a growing medical device company, is seeking a Supplier Quality Engineer to support supplier quality management activities and ensure the quality and compliance of externally sourced components and materials. This role will work closely with suppliers and internal cross-functional teams to address supplier nonconformances, drive corrective actions, and ensure suppliers meet regulatory and quality system requirements. The

If you’re the kind of Clinical Scientist who wants to own the story behind the data , not just contribute slides or sections, this role was built for you. Our start-up client is adding a Senior Clinical Scientist to take end-to-end ownership of the scientific and procedural documentation behind their structural heart device. This is a high

Our small medical device client is adding a Senior Manufacturing Quality Engineer to join their growing team. This is a critical role focused on leading our validation and verification efforts as they pursue ISO 13485, EU MDR, and CE Mark certifications. If you are a hands-on quality professional with a strong background in medical device manufacturing and a desire

Our early-stage medical device client is adding a Principal Design Assurance Engineer to the team. You’ll be the Design Quality voice from early concept through design transfer—helping teams build safe, compliant products without slowing innovation. This is a high-impact, cross-functional role partnering with R&D, Clinical, Ops, and Marketing to drive risk-based

Our dynamic, clinical-stage, fast-paced medical device startup is developing novel technologies with the potential to significantly change population health. Every team member is a key contributor, directly impacting the company's progress towards commercialization. They offer a challenging yet rewarding environment where individuals can thrive and see the direct impact of their work. Due to an internal promotion

We have partnered with a small start-up company that is looking for someone who’s hungry to grow, ready to learn, and excited to be at the center of product quality and regulatory excellence. In this role, you’ll be the bridge between engineering, manufacturing, quality, and regulatory teams, helping ensure their devices meet the highest standards and are

Our mid-sized medical device client is building a Program Management department. The Manufacturing Program Manager will oversee New Product Introductions, Capacity initiatives, and Transfer Programs. This role will work closely with plant leadership, quality, and the R&D group to create and establish a framework for oversight and management of NPI, Capacity Initiatives, and Transfer programs at manufacturing