Do you have an entrepreneurial mindset? Are you eager to contribute to the development of cutting-edge technology in patient monitoring devices? These devices enable patients and physicians to monitor health and improve outcomes, which are crucial to the medical device industry.

This is a great opportunity to be on the ground floor where you will have a key role in developing proof of concept and prototypes. If this is you, apply today!

Principal Biomedical Engineer Benefits:

• Salary: up to $200K – Top range going to individuals with entrepreneurial start-up leadership experience
• Fully remote role where you will work independently
• Comprehensive healthcare benefits
• The opportunity to be part of a growing startup with immense potential and a significant project pipeline

Principal Biomedical Engineer Qualifications:

• Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related field; a Master’s or Ph.D. is highly preferred.
• 7+ years of experience in medical device development, with at least 2 years in a leadership role.
• Early-stage start-up experience is required
• Strong knowledge of biomedical engineering principles, medical device design, and human factors engineering.
• Proficiency in CAD software, simulation tools, and statistical analysis.

Principal Biomedical Engineer Responsibilities:

• Product Development:
  • Lead the design, development, and testing of innovative medical devices, ensuring compliance with industry standards and regulations (e.g., FDA, ISO 13485).
  • Oversee the integration of biological, mechanical, and electronic components into functional prototypes and products.
  • Drive the development of technical documentation, including specifications, risk assessments, and validation reports.
  • Ensure manufacturability of prototype and final product.
• Innovation & Problem-Solving:
  • Identify and evaluate emerging technologies, materials, and processes to enhance product performance and competitiveness.
  • Troubleshoot design and manufacturing challenges, providing timely and cost-effective solutions.
• Regulatory Compliance & Quality Assurance:
  • Ensure all designs and processes meet regulatory and quality standards, including Good Manufacturing Practices (GMP) and risk management protocols.
  • Collaborate with regulatory specialists to prepare submissions and maintain compliance with international medical device standards.

At Goodwin Recruiting we are committed to our core values. We take our value, Dedicated to Diversity & Inclusion, very seriously and will never discriminate against a candidate or client based on any protected classes. Our clients seek qualified candidates, and that is what we deliver. A person's age, gender, race, sexual orientation, gender identity, national origin, veteran or disability status, or arrest or conviction record has no bearing on whether he, she, or they are able to do the job. We evaluate the knowledge, skills, and abilities that meet the requirements of the position and aim to open doors and change lives. We value all people, understanding that uniqueness and diversity foster a stronger team that is innovative and brings varying perspectives to the table. We put our money where our mouth is and are proud of our efforts to identify a broad slate of candidates, with many hiring success stories to share.   JOB ID: 150097 #post

Mitch Rachman