Electro-Mechanical Technician

As an Electro‑Mechanical Engineer, you will support the development, testing, validation, and commercialization of medical device components, assemblies, and equipment. This hands‑on role is highly collaborative, working closely with Engineering, R&D, Operations, and external suppliers to ensure new products and processes meet performance, quality, and regulatory requirements. You will play a critical role across the full product lifecycle—from prototyping and early development through validation, equipment runoff, and transition to manufacturing—while maintaining detailed documentation and supporting knowledge transfer within the organization.

Testing & Validation Support

• Perform acceptance testing on product prototypes and new products throughout the development lifecycle.
• Prepare, set up, execute, and tear down test configurations for components, subassemblies, and equipment.
• Operate both third‑party test equipment and Ethicon devices/systems.
• Conduct validation testing, equipment runoff, and acceptance testing for new equipment.
• Document test results clearly and communicate findings to the engineering team, including preparation of detailed reports and first‑level data analysis.
• Assist in developing and refining test procedures and protocols, recommending improvements based on available equipment and technical constraints.
• Maintain written test procedures, best practices, and documentation to support training and long‑term knowledge retention.
• Provide training and onboarding support for new testing personnel as needed.
• Apply basic engineering and statistical techniques, including process capability studies, validation protocols, and process validation activities.
• Develop solutions that meet defined quality, performance, and cost targets.

Prototyping & Process Development

• Build, maintain, and operate prototype, test, and production equipment.
• Support the installation, startup, debugging, and validation of new products and equipment.
• Manage hands‑on aspects of early‑stage development and engineering builds.
• Interface with equipment suppliers to ensure systems and components meet defined performance specifications.
• Collaborate with operations teams to ensure smooth transition of equipment and processes from prototype to production.
• Perform incoming equipment and component testing to meet internal quality requirements.
• Assist in creating, maintaining, and updating standard operating procedures (SOPs).
• Provide equipment and process training to both R&D and operations personnel.
• Support component qualification documentation and technical packets.
• Organize and conduct engineering builds.
• Support process development and qualification strategies for:
  • Components and component tooling
  • Assembly processes and equipment
  • Tools and gauges
  • Software‑driven systems

Logistics & Documentation Support

• Track equipment and component inventory throughout the product lifecycle.
• Manage equipment and component flow through the purchasing process to ensure on‑time delivery.
• Interface with internal procurement teams and external suppliers.

Required

• 3–5 years of experience in a regulated industry (medical device, pharmaceutical, aerospace, automotive, or similar).
• Hands‑on experience with testing, prototyping, validation, or manufacturing support.
• Ability to read and understand technical instructions, drawings, and specifications.
• Strong documentation and communication skills.
• Experience working with test equipment, mechanical systems, and electro‑mechanical assemblies.
• Comfort working in a lab, prototype, or production‑adjacent environment.
• Basic understanding of statistical methods and validation principles.

Preferred

• Associate’s degree (2‑year) in Engineering Technology, Electro‑Mechanical Technology, Mechatronics, or related technical field.
• Experience supporting FDA‑regulated or ISO‑compliant environments.
• Familiarity with process validation, equipment qualification, and component qualification processes.
• Experience transitioning products from R&D into manufacturing.
• Exposure to SOP development, training, and knowledge transfer processes.

Important Information

This position is recruited by a remote Kelly office, not your local Kelly branch. Applicants must be legally permitted to work in the United States.

Kelly is an equal opportunity employer including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity, and is committed to employing a diverse workforce. Equal Employment Opportunity is the law. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center.