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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.

PRODUCT DEVELOPMENT ENGINEER OVERVIEW:

This position is responsible for the design and development of medical devices device accessories and processes that complement our current product lines. This position also involves training Technicians Engineers Sales Representatives Customers etc. to processes and principles associated with the technology as well as providing ongoing technical support.

COMPETANCIES & RESPONSIBILITIES OF THE PRODUCT DEVELOPMENT ENGINEER:

Design and develop medical devices and accessories.

Use established procedures to improve existing medical devices and accessories. Continually optimize manufacturing procedures to produce less expensive higher quality medical devices.

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.

Assist in the completion of new and existing product design validations.

Complete design drawings in AutoCAD or similar drafting program and create prototypes to progress

the development through its design stages.

Assist in training PMT personnel to processes associated with design and development of medical

devices and accessories.

Work with production to 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.

Assist and support PMT Plastic customers from a technical standpoint.

Communicate with strategic vendors and suppliers.

QUALIFICATIONS:

2 or 4 year degree in applicable field of study preferably engineering (ME ChE EE BioMedE)

Minimum 2 years work experience in the medical device industry

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

Medical Surgical Laboratory Research/Equipment and Supplies Cosmetic

CONFIDENTIAL EQUAL OPPORTUNITY EMPLOYER

JOB CODE: PDEfeb2025