Senior Mechanical Engineer

Posted 7 Days Ago
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Minnetonka, MN, USA
Hybrid
Senior level
Healthtech • Manufacturing
The Role
Lead mechanical design and optimization of implantable neurostimulation devices, collaborate cross-functionally, prototype and iterate using 3D modeling, support verification/validation, design transfer to manufacturers, compile device history and risk/usability files, and assist regulatory filings and IP development.
Summary Generated by Built In

Saluda Medical is a commercial‑stage medical device company focused on developing treatments for chronic neurological conditions using its novel closed‑loop neuromodulation platform. The company’s proprietary technology senses and measures neural responses to stimulation and automatically adjusts therapy based on real‑time neurophysiological feedback.

Saluda Medical’s first product, the Evoke® System, is designed to deliver known, consistent, and personalized spinal cord stimulation therapy by objectively measuring neural responses and maintaining therapy within a prescribed therapeutic window. Saluda Medical is headquartered in Minneapolis, Minnesota.

At Saluda, we challenge boundaries. We innovate and think beyond the conventional. Our focus is to revolutionize the standard of care in neuromodulation to positively impact patient’s lives.

Saluda Medical seeks a Senior Mechanical Engineer to contribute to the development of advanced implantable Neurostimulation devices. This global role involves collaborating with diverse teams across various stages of product development, from research and development to manufacturing transfer. 

Responsibilities:

Device Design and Optimization: Lead the design, development, and optimization of neuro-lead interfaces and implantable medical devices to meet project goals and timelines. 

Cross-functional Collaboration: Collaborate closely with R&D, engineering, and clinical teams to ensure alignment of designs with project objectives, incorporating feedback from clinical trials and user studies. 

Innovation and Integration: Drive innovation by incorporating advanced modeling techniques, staying informed about industry trends, and ensuring the seamless integration of electrical stimulation and modulation techniques into implantable devices. 

 

Key Responsibilities: 

  • Design, prototype, and iterate on new implantable medical devices, incorporating feedback from clinical trials. 
  • Develop mechanical designs for next generation neurostimulators, considering complex electronics integration. 
  • Utilize 3D modeling and rapid prototyping techniques for early design iterations. 
  • Document designs thoroughly for verification and validation activities. 
  • Lead sub-projects and collaborate with external manufacturing teams for design transfer and production optimization. 
  • Compile and analyze operational data to establish technical specifications and ensure compliance with industry standards. 
  • Develop device history files including requirements, risk management, and usability files. 
  • Support regulatory filings and intellectual property development. 
  • Managing relationships with Contract Manufacturers providing guidance on process development 
  • Prior experience with labelling would be an advantage 

 

Qualifications: 

  • Bachelor's degree in engineering (Mechanical Engineering, Manufacturing Engineering, or related field). 
  • Experience with FDA regulations (21 CFR 820.30) and international standards (IEC 60601-1). 
  • Experience in R&D activities related to electro-mechanical implantable medical devices. 
  • Self-starter with the ability to work independently and collaboratively in a multidisciplinary environment. 

Saluda Medical embraces diversity and equal opportunity. We are committed to building a team representative of a variety of backgrounds, perspectives and skills. We believe people are the source of our inspiration and innovation.

Saluda Medical does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on Saluda Medical’s approved agency list. Unsolicited resumes or candidate information submitted to Saluda Medical by search/recruiting agencies not already on Saluda Medical’s approved agency list shall become the property of Saluda Medical.

Skills Required

  • Bachelor's degree in Mechanical, Manufacturing, or related Engineering field
  • Experience with FDA design control regulations (21 CFR 820.30)
  • Experience with international medical electrical safety standard IEC 60601-1
  • R&D experience with electro-mechanical implantable medical devices
  • Proficiency with 3D modeling and rapid prototyping techniques
  • Experience developing device history files, risk management, and usability files
  • Experience leading design transfer and collaborating with contract manufacturers
  • Ability to work independently and collaboratively in multidisciplinary teams (self-starter)
  • Prior experience with labeling
  • Experience supporting regulatory filings and intellectual property development
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The Company
Bloomington, , Minnesota
482 Employees
Year Founded: 2011

What We Do

Saluda Medical is a global company revolutionizing the field of neuromodulation with an emerging portfolio of therapies driven by advanced closed-loop technologies designed to treat debilitating neurological disorders. The company’s first product, the Evoke® System, is the only ECAP-controlled closed-loop spinal cord stimulation (SCS) system and is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with failed back surgery syndrome, intractable low back pain, and leg pain. The Evoke System instantaneously reads, records, and responds to the nerves’ response to stimulation to provide continually optimized therapy and is proven to be superior to open-loop SCS for the treatment of overall trunk and/or limb pain. 12-month results from the EVOKE Study, the first double-blind randomized controlled trial (RCT) used in support of Premarket Approval (PMA) in spinal cord stimulation history, were published in The Lancet Neurology and 24-month results have since been published JAMA Neurology. Both studies are poised to set new clinical standards for long-term pain relief and improvements in physical and emotional functioning, sleep quality and health-related quality of life. In the EU, Evoke is CE Marked and commercially available. In the U.S., Evoke is FDA-approved and will be available when the Company implements its full commercial release in 2023. Saluda Medical is a privately held company with headquarters in Bloomington, MN, USA. To learn more about Saluda Medical, including the risks & important safety information, visit www.saludamedical.com

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