Engineer II

Contract R&D Engineer II role with a global medical-device company. Start date: October 1st; 12-month contract; hybrid (3 days/week in Bloomington, IN).

About the role

Design, test, and technically document the feasibility, construction, and production process of new and/or changed medical products.

Responsibilities

• 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.
• Work and interact effectively and professionally with and for others throughout various levels of the global organization.
• Strictly adhere to safety requirements.
• Maintain regular and punctual attendance.
• Maintain company quality and quantity standards.
• Perform other duties as assigned.

Requirements

• Excellent problem-solving skills.
• Ability to work in collaborative and independent work situations and environments with minimal supervision.
• Ability to remain calm and receptive in fast-paced situations.
• Effective oral and written communication skills.

Pay

$55–65 per hour, depending on experience.

Schedule

Hybrid: 3 days per week in-office (Bloomington, IN).