×
Register Here to Apply for Jobs or Post Jobs. X

Principal Engineer​/Manager, Research & Development - MN

Job in Tampa, Hillsborough County, Florida, 33646, USA
Listing for: FloodGate Medical
Full Time position
Listed on 2026-01-16
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 192000 - 201000 USD Yearly USD 192000.00 201000.00 YEAR
Job Description & How to Apply Below

Venture Med Group

Venture Med Group is a pioneering medical device company focused on developing endovascular solutions for treating peripheral arterial disease (PAD) and stenoses in arteriovenous (AV) fistulas and grafts. Their flagship FLEX Vessel Prep™ System uses a non‑balloon, micro‑incision technology to optimize vessel preparation and improve outcomes when combined with revascularization therapies. With recent regulatory milestones and expanded clinical evidence, Venture Med is scaling its commercial footprint while reinforcing its commitment to better patient outcomes.

Why

You Should Join Us

This is a Principal Engineer/Manager, R&D role in Minnesota. The Principal Engineer/Manager of Research & Development is responsible for executing product development activities within the company’s medical device portfolio, including the Venous platform. This individual will lead efforts related to design controls, product verification and validation, and sustaining engineering to ensure products meet performance, safety, and regulatory requirements. The role requires a hands‑on engineer who can manage projects, collaborate across departments, and drive continuous improvement from concept through commercialization.

What

You’ll Do
  • Plan and execute product development activities, ensuring adherence to design control processes in compliance with FDA and ISO 13485 requirements.
  • Prepare and maintain design history files, risk management documentation, verification and validation protocols, and reports.
  • Lead design reviews and ensure all deliverables meet technical, quality, and regulatory expectations.
  • Collaborate closely with Operations, Quality, and Regulatory Affairs to ensure a smooth transfer from development to manufacturing.
  • Participate in product testing, verification, validation, and clinical evaluation support activities.
  • Support continuous improvement initiatives to enhance design processes, manufacturability, and product performance.
  • Evaluate customer and user feedback to drive design improvements and address post‑market needs.
  • Provide technical guidance and mentorship to junior engineers and technicians.
  • Manage project timelines, resources, and budgets to ensure on‑time and on‑scope execution.
  • Coordinate with suppliers and contract manufacturers to define component specifications, materials, and process requirements.
  • Ensure compliance with quality system requirements and participate in internal and external audits as needed.
  • Communicate effectively with cross‑functional stakeholders to align on priorities, milestones, and technical deliverables.
What You’ll Need
  • Bachelor’s degree in chemical, mechanical or biomedical engineering, or related discipline.
  • Minimum of 10 years of experience in medical device product development, including at least 5 years working under design controls.
  • Demonstrated knowledge of design control principles per 21 CFR 820 and ISO 13485 standards.
  • Experience leading verification and validation testing and compiling documentation for regulatory submissions.
  • Strong understanding of medical device manufacturing processes and design‑for‑manufacturability principles.
  • Proven track record managing multiple development projects from concept through design transfer.
  • Hands‑on experience in device design, prototyping, test method development, and 3D printing.
  • Excellence in problem‑solving and root cause investigations.
  • Previous ownership of design history file with experience producing all requisite documents including plans, protocols, reports, design specifications, traceability matrices, test methods, and build instructions.
  • Excellent written and verbal communication skills, with ability to lead technical discussions and prepare detailed documentation.
  • Highly organized, self‑motivated, and detail‑oriented professional capable of working both independently and collaboratively.
  • Experience in a 3D‑modelling software preferred.
  • Ability to travel up to ~20%.
Perks of the Job
  • Competitive base salary: $175k
  • Bonus:
    10–15%
  • Total Income: $192k–201k
  • Full health benefits (medical, dental, vision)
  • 401(k) plan
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary