Principal Mechanical Engineer

Veranex; Minneapolis (MN); On-site; USD 80,000 - 120,000; Full time

Job summary

Join a forward-thinking company as a Principal Mechanical Engineer, where your innovative designs will enhance patient care through cutting-edge medical technologies. In this dynamic role, you will lead the development of complex electro-mechanical devices, collaborating with global teams to ensure compliance with industry standards. With a focus on creativity and problem-solving, you'll manage multiple projects and drive product success in a regulated environment. This is an exciting opportunity to make a significant impact in the healthcare industry while working in a supportive and collaborative atmosphere.

Qualifications

• 6+ years of experience in medical device product development.
• Expertise in CAD design and prototype testing.

Responsibilities

• Lead design and development of electro-mechanical medical devices.
• Ensure compliance with FDA and ISO regulations.

Skills

Medical Device Development

Problem Solving

Communication Skills

Attention to Detail

Multi-tasking

Education

Bachelor's degree in Mechanical Engineering

Tools

SolidWorks

Microsoft Office

Job description

Veranex is the leading service provider for medtech companies. Our global team of experts help clients anticipate challenges and find solutions throughout the development and commercial lifecycle. Together, we accelerate new technologies to market and improve patient outcomes.

About This Role :

Veranex has an exciting opportunity to join the Mechanical Engineering Team as Principal Mechanical Engineer. You will be part of a team working to improve lives globally through healthcare innovation. You will lead and participate in mechanical design and development activities through all phases of the medical project development process, from the initial design effort, through testing and validation, and final manufacturing transfer. This role reports to the Manager of Mechanical Engineering and collaborates with Product Development & Engineering teams globally.

The ideal candidate should be an innovative, creative and well-organized self-starter, an expert problem solver, collaborative, and passionate about enhancing patient care and advancing the healthcare industry. They should have experience with medical device development or similar regulated industry. As a consultant, they should be comfortable working with clients as a trusted partner, managing risk-based decisions in the interest of project success. They should also possess excellent conceptual and analytical skills along with the ability to solve complex technical problems. Be able to effectively manage multiple tasks and projects and resolve a wide range of problems in creative ways. They must work independently with minimal guidance.

What You Will Do

• Executes the design and development of complex electro-mechanical medical devices and equipment. Participates in a variety of manufacturing

processes, including injection molding of plastics, machining methods, rapid prototyping techniques, etc.

• Develops expert level detailed computer-aided design (CAD) packages to include 3D data and 2D drawings.
• Maintains day-to-day communication with program managers and all appropriate program team members.
• Researches and procures sample components and develops high-functioning design prototypes. Develops and executes prototype testing plans and protocols.
• Ensures innovative product design that will exceed client expectations and succeed in the marketplace.
• Ensures compliance with medical device regulations and standards.
• Directs and leads internal resources and manage external development partners
• Provides leadership, training, guidance, and support to mechanical engineering staff
• Participates in business development activities by reviewing proposal content and attending sales calls
• Functions as mechanical engineering lead on product development programs.
• Utilize in-depth knowledge of product development and overall medical device industry Food & Drug Administration (FDA), Quality System Regulation (QSR) and International Organization for Standardization (ISO) regulations

Qualifications

Required skills :

• Bachelor's degree in Mechanical Engineering
• 6+ years relevant work experience
• Strong knowledge of medical device product development
• Strong knowledge in Microsoft Office and SolidWorks
• Excellent written and verbal communication skills.
• Excellent attention to detail
• Multi-tasking and time management skills with the ability to prioritize tasks.

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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Principal Mechanical Engineer • Minneapolis, MN, United States