Description:

• Performs research and engineering functions involving the layout, building, testing, troubleshooting, repairing and modification of, but not limited to, cardiac lead assemblies and implantable medical devices.
• Performs a variety of duties in the electrical, mechanical, electro-mechanical, chemical, or optical areas.
• Constructs, operates, troubleshoots, calibrates, adjusts, maintains, and tests equipment, systems, or products.
• Works from schematics, engineering drawings, and written or verbal instructions.
• Performs tests, analyzes data, and writes reports.
• Reviews and/or develops processing and/or manufacturing instructions.
• Maintains detailed documentation through all phases of development, testing and analysis.
• Plans and organizes non-routine tasks with approval.
• Initiates or maintains build/project schedule and establishes priorities of work assignments with management input.
• Solves a wide range of problems requiring some interpretation of defined procedures and practices.
• Selects methods and practices with guidance from supervisor to obtain imaginative, thorough, and practical solutions to questions.
• Maintains general knowledge of products/services associated with area and employees involved with specific product lines and services.
• Validate components and fixtures following receiving inspection standard procedures.

Qualifications:

• H.S. diploma or equivalent.
• 3-5 years of medical device (or similar field) manufacturing/assembly experience and/or 2 years of experience in technician trade or equivalent technician experience.
• Receive general instructions and able to work independently and efficiently without direct guidance, solve challenges, and appropriately relay concerns to management when needed.
• Exercises judgment within defined procedures and practices to determine appropriate action.
• Understands timelines and ensures deadlines are met with high quality work. Responsible for completing project tasks successfully within time and budget constraints.
• Perform routine and non-routine moderately complex assignments using standard methods and sequences.
• Make adjustments, modifications, and replacements to set processes as directed. Able to find and reach out to other subject matter experts to find solutions as necessary.
• Assignments require broad judgment in troubleshooting proven processes as well as the ability to suggest alternatives.
• Work in a stringent quality system environment. Work experience in the medical industry under FDA regulation preferred.
• Good communication skills, both written and verbal required.
• Interacts well with diverse groups and maintains strong working relationships with internals in a collaborative, fast-paced, goal-driven environment.
• Listens to and understands others’ points of view; possesses interpersonal skills to negotiate and reconcile differences.
• Exercises discretion regarding work details.
• Coordinates efforts with technical and support staff.
• Ability to utilize a SmartScope or other CMM a plus.
• Experience with validating raw materials, parts, or components through receiving inspection a plus.

Job Type: Contract

Pay: Up to $31.00 per hour

Schedule:

• 8 hour shift

Experience:

• medical devices: 2 years (Required)
• troubleshooting: 2 years (Required)

Work Location: On the road