Job Description
Job DescriptionAbout Us
We’re more than a startup—we’re building the future of medical innovation. If you thrive in a collaborative environment, take ownership of your work, and are motivated by making a real impact, you’ll fit right in.
Every team member plays a key role in advancing technologies that improve patient outcomes. We foster a culture where your ideas are valued, your growth is a priority, and your contributions directly shape our success.
The Opportunity
We’re looking for a driven Senior R&D Engineer with heart valve expertise to join our team. In this role, you’ll work cross-functionally to support the design and development of a TMVR system, with a strong focus on valve technologies.
This position requires deep technical knowledge, an understanding of clinical and regulatory requirements, and the ability to lead development efforts, influence technical decisions, and drive continuous improvement.
What You’ll Do
Product Development
- Lead the design and development of innovative heart valve technologies
- Translate customer needs into product requirements
- Develop and validate test methods, fixtures, and protocols (hydrodynamic, accelerated wear, tissue testing, etc.)
- Partner with Manufacturing on technology transfer, scale-up, and process improvements
Technical Leadership
- Build deep expertise in cardiovascular anatomy, heart valve technologies, and regulatory requirements
- Troubleshoot challenges, perform root cause analysis, and contribute to design reviews
Testing & Analysis
- Plan and execute bench testing, engineering studies, and preclinical evaluations
- Lead verification and validation efforts for regulatory submissions
- Analyze data and communicate findings to drive informed decisions
Regulatory & Quality
- Collaborate with Regulatory Affairs to ensure compliance with applicable standards
- Support submission preparation
- Partner with Quality to maintain strong testing, validation, and quality control processes
Project Management
- Develop and manage project plans, timelines, and deliverables
- Identify risks and proactively mitigate them
- Communicate progress and challenges clearly to stakeholders
- Work cross-functionally across R&D, Quality, Regulatory, and Manufacturing to stay aligned
What You Bring
Minimum Qualifications
- Bachelor’s degree in Mechanical, Biomedical Engineering, or related field (Master’s/PhD preferred)
- 5+ years of engineering/product development experience
- 3+ years in medical devices (preferably interventional or implantable)
What Sets You Apart
- Experience designing and testing complex medical devices
- Strong problem-solving and technical leadership capabilities
- Background in heart valve or structural heart technologies (highly preferred)
- Knowledge of cardiovascular anatomy and physiology
- Familiarity with materials and manufacturing processes (nitinol, tissue, extrusion, laser, etc.)
- Experience with design controls, risk management, and ISO 13485/FDA QSR
- Proficiency with CAD (SolidWorks), FEA, and data analysis tools (Minitab)
- Strong communication skills with the ability to present to both technical and non-technical audiences
- Proven ability to collaborate across teams and manage complex projects
Why Join
We offer competitive compensation and a comprehensive benefits package to support you and your family:
- Medical, Dental, Vision
- FSA
- Life Insurance
- 401(k)
- Paid Holidays & PTO
- Paid Parental Leave
We are an equal opportunity employer committed to building a diverse and inclusive workplace.
Job Type & Location
This is a Permanent position based out of Maple Grove, MN.
Pay and Benefits
The pay range for this position is $105000.00 - $150000.00/yr.
We recognize that meaningful work is supported by meaningful benefits. That’s why we offer a competitive compensation package along with comprehensive benefits designed to support you and your family’s health, well-being, and financial future. Our benefits package includes:
• Medical
• Dental
• Vision
• Flexible Spending Account (FSA)
• Basic Life
• 401(k) Retirement Plan
• Paid Holidays
• PTO
• Maternity/Paternity paid leave It is 4C Medical’s policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state or local laws.
Workplace Type
This is a fully onsite position in Maple Grove,MN.
Application Deadline
This position is anticipated to close on May 21, 2026.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.
About Actalent
Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.
Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.