Job Description

LOOKING FOR AN ENERGETIC PROFESSIONAL COMING FROM A REGULATED ENVIRONMENT!

• Generates detailed models/drawings and functional prototypes based on theoretical concepts.
• Implements drafting standards to maintain consistency in notes, layout and dimensioning schemes.
• Builds and tests prototype devices.
• Selects materials for component parts and medical devices.
• Provides technical input for projects at all stages of the product life cycle.
• Translates User Needs into Design Input Requirements to comply with regulatory requirements and best-practice standards.
• Participates in Design Verification activities to ensure Design Outputs satisfy Design Input Requirements.
• Leads one or more product development projects for medical devices to achieve on-time results and according to plan.
• Maintains Design Controls documentation in accordance with established regulatory requirements and SOPs.
• Assesses new technologies and new product ideas for technical feasibility.
• Assists in the design of test apparatuses/equipment and the development of procedures for testing products including setting acceptance criteria.
• Provides engineering support for products launching to production and resolves issues as they arise.

Qualifications

OUR EXPECTATIONS

• Bachelors Degree
• 5 to 10 years of experience designing from concept through production. 
• Experience implementing Design for Manufacturability (DFM) principles into design.
• Experience with industrial design and human factors engineering strongly preferred.
• Strong mechanical, analytical and problem solving skills.
• Creative with strong attention to detail.
• Ability to manage multiple projects with sometimes conflicting priorities.
• Excellent communication and interpersonal skills to interact with clinicians, engineers and team members.
• Ability to work independently and with others in a fast-paced, results oriented environment.

Additional Information

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Compensation:  $95,000 - $105,000 + 10% bonus, weeks of PTO and great benefits