What are the responsibilities and job description for the Sr. Biomedical Engineer position at PMT Corporation?
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PMT Corporation, located in Chanhassen, Minnesota, is known for manufacturing and distributing high end, innovative products within the Orthopedic, Neurosurgery, and Plastic Surgery markets. Our workplace is a community of innovators who are passionate about creating an impact. We recognize that the collective power of our team is what propels us forward. Together, we celebrate successes, learn from challenges, and continuously evolve in our pursuit of excellence.
Join us at PMT Corporation if you're ready to be a part of a collaborative, idea-driven, and communicative environment. Your innovation matters, and together, we can continue to shape the future of the medical device industry.
| SR. BIOMEDICAL ENGINEER OVERVIEW:
We are looking for an experienced Biomedical Engineer with a strong background in product development to join our team at PMT Corporation. This role will be leading the design, development, and testing of innovative medical devices and accessories. This position requires both working individually as well as collaborating with cross-functional teams to ensure our products meet regulatory standards and address real-world medical needs. |
| COMPETANCIES & RESPONSIBILITIES OF THE SR. BIOMEDICAL ENGINEER:
· Lead the design and development of medical devices from concept through production · Collaborate with cross-functional teams such as R&D, Quality Assurance, Regulatory Affairs, Production, etc. to ensure product compliance within regulatory requirements · Perform test procedures to verify and validate product quality and efficacy. · Document all developments in scientific notebooks complete Engineering Change Orders (ECOs) document and control processes and procedures. · Leads and/or oversees assigned projects, collaborating with stakeholders to achieve targeted outcomes · Complete design drawings in AutoCAD or similar drafting program and create prototypes to progress development through its design stages. · Assist in training PMT personnel such as Technicians, Engineers, Sales Representatives, Customers, etc. in processes associated with design and development of medical devices and accessories. · Develop efficient (i.e. cost, material, time, etc.), user-friendly manufacturing processes. · To assist in the resolution, documentation, customer responses of product complaints. · Coordinate and assist in corrective and preventative action activities and solutions · Comply with appropriate regulatory agencies (i.e. GMP, ISO, FDA, etc.) and associated quality systems described in PMT’s documentation. · Communicate with strategic vendors and suppliers. |
| QUALIFICATIONS OF THE SR. BIOMEDICAL ENGINEER:
· 4 year degree in applicable field of study, Master’s degree preferred · 5-10 years’ work experience in the medical device industry · Strong product development skills, specifically ability to work with Production throughout design, development, and testing of devices and accessories · Excellent written and verbal communication skills · Self-starter and self-organizer · Successful with project management · Exceptional problem solving and design skills · Strong personal computer skills, including experience with MS Office, Solidworks, AutoCad, MS Project · Able to pass background and drug screenings |
