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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 youre ready to be a part of a collaborative ideadriven 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 crossfunctional teams to ensure our products meet regulatory standards and address realworld medical needs.
COMPETANCIES & RESPONSIBILITIES OF THE SR. BIOMEDICAL ENGINEER:
Lead the design and development of medical devices from concept through production
Collaborate with crossfunctional 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. userfriendly 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 PMTs documentation.
Communicate with strategic vendors and suppliers.
QUALIFICATIONS OF THE SR. BIOMEDICAL ENGINEER:
4 year degree in applicable field of study Masters degree preferred
510 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
Selfstarter and selforganizer
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
Required Experience:
Senior IC
Full Time