The primary purpose of this position is to design, test and technically document the feasibility, construction and production process of new and / or changed medical products.
ESSENTIAL JOB FUNCTIONS / DUTIES
- Design new product ideas as assigned by VP of Engineering
- Build and test new product prototypes
- Document the final product design
- Assist in writing design and specification documentation for
FDA application
- Initiate and oversee the pre-production run of new products
- Plan the ongoing production of the product
- Consult with Production personnel for device changes / updates as necessary.
- Maintain a design file for each new product and turn that file over at product completion for permanent records.
- Call on vendors to assess raw materials.
- Call on physicians to discuss product ideas or evaluations.
- Attend various trade shows to source raw materials or to attend Company exhibitions.
- Must work and interact effectively and professionally with and for others
throughout various levels of the global organization
- Must strictly adhere to safety requirements
- Maintain regular and punctual attendance
- Must maintain company quality and quantity standards
- Must have effective oral and written communication skills
- Excellent problem solving skills and ability to work in collaborative and
independent work situations and environments with minimal supervision
- Ability to remain calm and receptive in fast paced situations
- Other duties as assigned
MINIMUM WORK EXPERIENCE / EDUCATIONAL REQUIREMENTS
- Minimum 4 year degree in Engineering / Technology.
- Ability to work independently and remain self-motivated.
- Experience and understanding of the validation process.
- Ability to travel 25% of the time.
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